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(-)-DIOP

Product Name
(-)-DIOP
CAS No.
32305-98-9
Chemical Name
(-)-DIOP
Synonyms
(R)-DIOP;(-)-Diop;(R,R)-DIOP;(4R,5R)-DIOP;phosphino)butane;(-)-2,3-O-IsopropyL;(2r,3r)-(-)-1,4-Bis(Diphenyl;idene-2,3-dihydroxy-1,4-bis(diphenyL;(4R,5R)-(-)-4,5-BIS(DIPHENYLPHOSPHINOMET;(3-chloro-2-hydroxypropyl) dihydrogen phosphate
CBNumber
CB3371576
Molecular Formula
C31H32O2P2
Formula Weight
498.54
MOL File
32305-98-9.mol
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(-)-DIOP Property

Melting point:
88-90 °C(lit.)
alpha 
-26° (c 2.0, CHCl3)
Boiling point:
590.3±25.0 °C(Predicted)
storage temp. 
2-8°C
form 
Powder
color 
white
optical activity
[α]19/D 26°, c = 2.3 in chloroform
Sensitive 
Air Sensitive
BRN 
1441045
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37
WGK Germany 
3
10-23
TSCA 
No
HS Code 
29329990
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
237655
Product name
(?)-2,3-O-Isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane
Purity
98%
Packaging
1g
Price
$259.7
Updated
2025/07/31
TCI Chemical
Product number
B1113
Product name
(2R,3R)-(-)-1,4-Bis(diphenylphosphino)-2,3-O-isopropylidene-2,3-butanediol
Purity
>97.0%(T)
Packaging
1g
Price
$132
Updated
2021/12/16
Strem Chemicals
Product number
15-2970
Product name
(4R,5R)-(-)-4,5-Bis(diphenylphosphinomethyl)-2,2-dimethyl-1,3-dioxolane, 99.5% (R,R)-DIOP
Packaging
250mg
Price
$57
Updated
2024/03/01
Strem Chemicals
Product number
15-2970
Product name
(4R,5R)-(-)-4,5-Bis(diphenylphosphinomethyl)-2,2-dimethyl-1,3-dioxolane, 99.5% (R,R)-DIOP
Packaging
1g
Price
$139
Updated
2024/03/01
TRC
Product number
D494003
Product name
(-)-DIOP
Packaging
10mg
Price
$45
Updated
2021/12/16
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(-)-DIOP Chemical Properties,Usage,Production

Chemical Properties

white powder

Uses

For the in situ preparation of chiral hydrogenation catalysts.

General Description

(-)-2,3-O-Isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane is a C2 chelating diphosphine ligand for transition metal complexes during asymmetric catalysis.

Synthesis

4376-01-6

37002-45-2

32305-98-9

In a 250 mL three-necked round-bottomed flask fitted with a PTFE stirrer, a coated stirring bar, a thermometer and its adapter, a reflux condenser with a gas inlet at the top, and a device with a 60 mL dosing funnel and PTFE Claisen fittings were assembled. The sample port of the plug valve was heated using a hot air gun and simultaneously purged with a rapid nitrogen stream to degas. 16.0 g (36.1 mmol) of (-)-1,4-di-O-toluenesulfonyl-2,3-O-isopropylidene-L-threitol (CAS No. 37002-45-2, also known as bis(toluenesulfonate)) was added to the reactor and purged with a nitrogen purge for an additional 30 min. Bis(toluene sulfonate) was dissolved in 100 mL of degassed anhydrous tetrahydrofuran. The sodium diarylphosphide solution prepared in step 2) was transferred to a 60 mL addition funnel through a cannula and added dropwise at a rate to a rapidly stirred solution of bis(toluene sulfonate), keeping the reactor temperature below 40 °C. Upon addition of the electrophilic reagent, the solution was reddish-orange in color and the diaryl phosphide salt disappeared rapidly to form a beige suspension. After dropwise addition, the oil bath was placed below the reactor and heated to 50 °C for 45 min to complete the phosphide coupling step. Subsequently, the Claisen adapter assembly was replaced with a short-range distillation head and approximately 50% of the tetrahydrofuran was removed by distillation. Phase separation was achieved by adding 100 mL of degassed heptane and water. The two-phase solution was filtered through an inert glass sintered funnel to remove carbon black and the lower aqueous phase was removed through a cannula. The upper organic phase was washed with 50 mL of degassed water and the aqueous phase was again removed through a cannula. Next, the organic heptane phase was extracted with 100 mL of anhydrous degassed acetonitrile, the lower acetonitrile phase was removed through a cannula, and the extraction was repeated once more with 50 mL of degassed acetonitrile. The acetonitrile phases were combined and transferred to a single-necked round-bottomed flask with a polytetrafluoroethylene stopcock valve and 24/40 standard conical ground glass fittings. The volatiles were removed on a rotary evaporator to give a viscous orange-brown glassy solid, which was further dried under vacuum. In the drying oven, the plug valve was replaced with a PTFE Claisen adapter with reflux condenser and gas inlet. The glassy solid was dissolved in 100 mL of degassed methanol, introduced via cannula or syringe, and heated to reflux to completely dissolve the ligand. Heating was stopped and the flask was immersed in an ice bath and cooled to -10 °C to give a white to off-white/beige solid. The solid DIOP ligand was collected through a glass sintered Schlenck filter, washed with cooled methanol, and dried overnight under vacuum. A final 11.7 g (23.5 mmol, molecular weight 498.34 g/mol) of (-)-DIOP ligand was obtained. The ligand was analyzed by 1H NMR (CDCl3: δ = 7.58-7.29 ppm, multiple peaks, 20H, aromatic; δ = 4.0-3.8 ppm, double peaks, 2H, -CH-; δ = 2.50-2.25 ppm, multiple peaks, 4H, -CH2-; δ = 1.35 ppm, single peaks, 6H, -CH3), 13C NMR (data not shown but consistent with the target product) and 31P NMR (CDCl3: δ=-22.87 ppm, single peak) for characterization. The molar percent P purity was >99%, and the total phosphorus content was determined by ICP to be 12.2 wt% P (theoretical value of 12.4 wt% P), indicating a chemical purity of approximately 98.4%, with a molecular formula of C31H32P2O2 and a molecular weight of 498.34 g/mol.

Purification Methods

It has been recrystallised from *C6H6/pet ether. After 2 recrystallisations from EtOH, it was pure by TLC on silica gel using Me2CO/hexane as solvent. [Kagan & Dang J Am Chem Soc 94 6429 1972.] Lanthanide shift reagents See in “Aliphatic Compounds”, Chapter 4, europium (III) acetate above and Eu(tmc)3 and Eu(tfc)3 below.

References

[1] Patent: US2010/234642, 2010, A1. Location in patent: Page/Page column 13

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(-)-DIOP Suppliers

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
Beijing Donghualituo Techonlogy Development Co.,Ltd.
Tel
010-88425576
Fax
(+86)-10-88425546
Email
sales@dhltchem.com
Country
China
ProdList
793
Advantage
59
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Ark Pharm, Inc.
Tel
847-367-3680
Fax
847-367-3681
Email
sales@arkpharminc.com
Country
United States
ProdList
1670
Advantage
56
Beijing HwrkChemical Technology Co., Ltd
Tel
18515581800 18501085097
Fax
010-89508210
Email
sales.bj@hwrkchemical.com
Country
China
ProdList
9400
Advantage
55
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44801
Advantage
61
Shanghai Longsheng chemical Co.,Ltd.
Tel
021-58099652-8005 13585536065
Fax
021-58099609
Email
bin.wu@shlschem.com
Country
China
ProdList
9883
Advantage
59
Maya High Purity Chemicals
Tel
+86 (573) 82222445 (0)18006601000 452520369
Fax
+86 (573) 82222643
Email
sales@maya-r.com
Country
China
ProdList
11707
Advantage
57
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View Lastest Price from (-)-DIOP manufacturers

Hebei Chuanghai Biotechnology Co., Ltd
Product
(-)-DIOP 32305-98-9
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
20 mt
Release date
2025-03-12
Chemwill Asia Co.,Ltd.
Product
(-)-DIOP (-)-2,2-dimethyl-4,5-((diphenylphosphino)dimethyl)dioxolane 32305-98-9
Price
US $6.00/kg
Min. Order
1kg
Purity
High quality Professional Factory
Supply Ability
Ms Ella chemwill_asia@126.com www.chemwill.com
Release date
2019-04-04
Career Henan Chemical Co
Product
(-)-DIOP 32305-98-9
Price
US $1.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
1kg,5kg,100kg
Release date
2019-08-08

32305-98-9, (-)-DIOPRelated Search:


  • (2r,3r)-(-)-1,4-Bis(Diphenyl
  • (-)-2,3-O-Isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane, 98% 1GR
  • (4R,5R)-(-)-4,5-Bis(diphenylphosphinoMethyl)-2,2-diMethyl-1,3-dioxolane,99% (R,R)-DIOP
  • (4R,5R)-(-)-Bis(diphenylphosphinomethyl)-2,2-dimethyl-1,3-dioxolane (-)-DIOP (2R,3R)-(-)-2,3-O-Isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane
  • )-2,3-O-Isopropylidene-2,3-dihydroxy-1,4-bis(dipheny
  • (4R,5R)-(-)-2,2-Dimethyl-4,5-bis((diphenylphosphino)methyl)-1,3-dioxolane
  • (4R,5R)-(-)-4,5-Bis(diphenylphosphinoMethyl)-2,2-diMethyl-1,3-dioxolane,(R,R)-DIOP.
  • (-)-DIOP (-)-2,2-dimethyl-4,5-((diphenylphosphino)dimethyl)dioxolane
  • (4R,5R)-(-)-4,5-BIS(DIPHENYLPHOSPHINOMET
  • (-)-2,3-O-Isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)
  • 1,1'-[[(4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-diyl]bis(methylene)]bis[1,1-diphenylphosphine],99%e.e.
  • (4R,5R)-(-)-4,5-Bis(diphenylphosphinomethyl)-2,2- dimethyl-1,3-dioxolane for synthesis
  • (4R,5R)-DIOP
  • (4R,5R)-trans-4,5-Bis[(diphenylphosphino)methyl]-2,2-dimethyl-1,3-dioxolane
  • (R)-DIOP
  • Isopropenyl-2,3-dihydroxy-1,4-Bis (diphenylphosphino) butane
  • 1,1'-[[(4R,5R)-2,2-dimethyl-1,3-dioxolane-4,5-diyl]bis(methylene)]bis[1,1-diphenyl-Phosphine
  • (-)-2,2-dimethyl-4,5-((diphenylphosphino)dimethyl)dioxolane
  • (-)-2,3-O-Isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane 98%
  • (-)(2,3-O-isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane) OR (-)DIOP
  • (4R-TRANS)-[(2,2-DIMETHYL-1,3-DIOXOLANE-4,5-DIYL)BIS(METHYLENE)]BIS(DIPHENYLPHOSPHINE)
  • (-)-O-ISOPROPYLIDENE-2,3-DIHYDROXY-1,4-BIS(DIPHENYLPHOSPHINO)BUTANE
  • (R,R)-(-)-2,3-O-ISOPROPYLIDENE-2,3-DIHYDROXY-1,4-BIS(DIPHENYL-PHOSPHINO)BUTANE
  • (R,R)-DIOP
  • (3-chloro-2-hydroxypropyl) dihydrogen phosphate
  • (4R,5R)-(-)-4,5-Bis(diphenylphosphinomethyl)-2,2-dimethyl-1,3-dioxolane,99.5%(R,R)-DIOP
  • Phosphine, (4R,5R)-2,2-dimethyl-1,3-dioxolane-4,5-diylbis(methylene)bisdiphenyl-
  • (-)-2,3-O-ISOPROPYLIDENE-2,3-*DIHYDROXY- 1,4-BIS(DIP
  • (-)-1,4-Bis-(diphenylphosphino)-2,3-dihydroxy-2,3-
  • (-)-DIOP, (-)-2,3-O-Isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane, (4R,5R)-4,5-Bis(diphenylphosphino-methyl)-2,2-dimethyl-1,3-dioxolane
  • (R,R)-DIOP, (-)-1,4-Bis(diphenylphosphino)-1,4-dideoxy-2,3-O-isopropylidene-L-threitol, (4R,5R)-4,5-Bis(diphenylphosphino-methyl)-2,2-dimethyl-1,3-dioxolane, (4R-trans)-[(2,2-Dimethyl-1,3-dioxolane-4,5-diyl)bis(methylene)]bis(diphenylphosphine)
  • (4R)-2,2-Dimethyl-4β,5α-bis(diphenylphosphinomethyl)-1,3-dioxolane
  • [(4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-diyl]bis(methylene)bis(diphenylphosphine)
  • [[(4R)-2,2-Dimethyl-1,3-dioxolane-4β,5α-diyl]bis(methylene)]bis(diphenylphosphine)
  • 2,2-Dimethyl-4β,5α-bis(diphenylphosphinomethyl)-1,3-dioxolane
  • (-)-1,4-BIS(DIPHENYLPHOSPHINO)-1,4-DIDEOXY-2,3-O-ISOPROPYLIDENE-L-THREITOL
  • (2R,3R)-(-)-2,3-O-ISOPROPYLIDENE-2,3-DIHYDROXY-1,4-BIS(DIPHENYLPHOSPHINO)BUTANE
  • (2R,3R)-(-)-1,4-BIS(DIPHENYLPHOSPHINO)-2,3-O-ISOPROPYLIDENE-2,3-BUTANEDIOL
  • (4R,5R)-(-)-BIS(DIPHENYLPHOSPHINOMETHYL)-2,2-DIMETHYL-1,3-DIOXOLANE
  • (4R 5R)-(-)-O-ISOPROPYLIDENE-2,3-DIHYDROXY-1,4-BIS(DIPHENYLPHOSPHINO)BUTANE
  • (4R,5R)-(-)-4,5-BIS(DIPHENYLPHOSPHINOMETHYL)-2,2-DIMETHYL-1,3-DIOXOLANE
  • (4R,5R)-4,5-BIS(DIPHENYLPHOSPHINO-METHYL)-2,2-DIMETHYL-1,3-DIOXOLANE
  • (2R,3R)-(-)-1,4-Bis(diphenylphosphino)-2,3-O-isopropylidene-2,3-butanediol[(-)-DIOP]
  • (2R,3R)-(-)-1,4-Bis(diphenylphosphino)-2,3-O-isopropylidene-2,3-butanediol &gt
  • (4R,5R)-(-)-2,2-Dimethyl-4,5-bis((diphenylphosphino)methyl)-1,3-dioxolane, 97%, for synthesis
  • (-)-2,3-O-IsopropyL
  • idene-2,3-dihydroxy-1,4-bis(diphenyL
  • phosphino)butane
  • [(4R,5R)-5-(diphenylphosphanylmethyl)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl-diphenylphosphane
  • Phosphine, 1,1'-[[(4R,5R)-2,2-dimethyl-1,3-dioxolane-4,5-diyl]bis(methylene)]bis[1,1-diphenyl-
  • (4R,5R)-(-)-2,2-Dimethyl-4,5-bis((diphenylphosphino)methyl)-
  • (-)-Diop
  • (-)-2,3-O-Isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane
  • (R,R)-DIOP/(4R,5R)-(-)-4,5-Bis(diphenylphosphinomethyl)-2,2-dimethyl-1,3-dioxolane
  • (4R,5R)-(-)-4,5-Bis(diphenylphosphinomethyl)-2,2-dimethyl-1,3-dioxolane,98% (R,R)-DIOP
  • 1,1'-[[(4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-diyl]bis(methylene)]bis[1,1-diphenylphosphine
  • (?)-2,3-<i>O</i>-Isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)butane
  • (-)-2,3-O-Isopropylidene-2,3-dihydroxy-1,4-bis(diphenylphosphino)