ChemicalBook > CAS DataBase List > TRIS(1-PYRROLIDINYL)PHOSPHINE 97

TRIS(1-PYRROLIDINYL)PHOSPHINE 97

Product Name
TRIS(1-PYRROLIDINYL)PHOSPHINE 97
CAS No.
5666-12-6
Chemical Name
TRIS(1-PYRROLIDINYL)PHOSPHINE 97
Synonyms
Tripyrrolidinophsphine;Tripyrrolidinophosphine;Tripyrrolidine phosphine;Tris(pyrrolidino)phosphine;Tri(1-pyrrolidinyl)phosphine;Tri(pyrrolidin-1-yl)phosphine;Tris(N-pyrrolidinyl)phosphine;Tri(pyrrolidin-1-yl)phosphane;phosphorous acid tripyrrolidide;TRIS(1-PYRROLIDINYL)PHOSPHINE 97
CBNumber
CB8504337
Molecular Formula
C12H24N3P
Formula Weight
241.31
MOL File
5666-12-6.mol
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TRIS(1-PYRROLIDINYL)PHOSPHINE 97 Property

Boiling point:
104 °C/0.1 mmHg (lit.)
Density 
1.041 at 25 °C 1.049 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.53(lit.)
Flash point:
>230 °F
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
liquid
pka
9.74±0.20(Predicted)
Appearance
Colorless to light yellow Liquid
BRN 
1343311
InChI
InChI=1S/C12H24N3P/c1-2-8-13(7-1)16(14-9-3-4-10-14)15-11-5-6-12-15/h1-12H2
InChIKey
PXFLCAQHOZXYED-UHFFFAOYSA-N
SMILES
P(N1CCCC1)(N1CCCC1)N1CCCC1
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
775444
Product name
Tris(1-pyrrolidinyl)phosphine
Purity
97%
Packaging
500mg
Price
$52
Updated
2025/07/31
Sigma-Aldrich
Product number
775444
Product name
Tris(1-pyrrolidinyl)phosphine
Purity
97%
Packaging
2.5g
Price
$403
Updated
2025/07/31
American Custom Chemicals Corporation
Product number
ING0008286
Product name
TRIPYRROLIDINOPHOSPHINE
Purity
97.00%
Packaging
5MG
Price
$504.05
Updated
2021/12/16
Oakwood
Product number
475197
Product name
Tris(1-pyrrolidinyl)phosphine
Packaging
5g
Price
$100
Updated
2021/12/16
Oakwood
Product number
475197
Product name
Tris(1-pyrrolidinyl)phosphine
Packaging
1g
Price
$30
Updated
2021/12/16
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TRIS(1-PYRROLIDINYL)PHOSPHINE 97 Chemical Properties,Usage,Production

Uses

Monodentate P-donor ligand.

Used as a phosphitylation reagent for oligonucleotide synthesis.

Synthesis Reference(s)

Tetrahedron Letters, 29, p. 5983, 1988 DOI: 10.1016/S0040-4039(00)82246-7

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand

Synthesis

123-75-1

5666-12-6

4.3.1. Synthesis of tert-butyliminotris(1-pyrrolidinyl)orthophosphine. All operations were carried out under dry argon protection using freshly distilled dry solvents. In a 1L three-necked round-bottomed flask equipped with a PTFE-coated magnetic stirring bar, thermometer, dropping funnel, and argon inlet, freshly distilled pyrrolidine (85.20 g, 1.198 mol) and THF (300 mL) were added, and the mixture was cooled to -40°C. Subsequently, PCl3 (20.05 g, 0.146 mol) was added slowly and dropwise at -40°C in THF (200 mL) solution. After the dropwise addition, the reaction mixture was slowly warmed to room temperature and stirred at room temperature for 18 hours. Upon completion of the reaction, the solvent was removed under vacuum at room temperature and 50 mbar pressure and the solid residue was washed twice with hexane (2 x 100 mL). The hexane layers were combined and concentrated under vacuum at room temperature and 50 mbar pressure to afford tris(1-pyrrolidinyl)phosphine (29.34 g, 0.122 mol) as a colorless liquid. The resulting phosphine was transferred to a 250 mL three-necked round-bottomed flask equipped with a PTFE-coated magnetic stirring bar, a thermometer, a dropping funnel, and an argon inlet, cooled to 5°C, and tert-butyl azide (14.5 g, 0.146 mol) was added dropwise. The reaction mixture was stirred overnight at room temperature and subsequently heated to 85°C for 1 hour and cooled to room temperature. The volatiles were removed at 50 mbar pressure for 30 min. BaO (1.0 g) was added and the reaction mixture was heated at 140°C for 40 hours. Finally, the target product P1-base (29.1 g, 64% yield) was obtained by vacuum distillation over BaO.

References

[1] Journal of the American Chemical Society, 2003, vol. 125, # 4, p. 940 - 950
[2] European Journal of Organic Chemistry, 2013, # 9, p. 1811 - 1823
[3] Journal of Organic Chemistry, 1994, vol. 59, # 6, p. 1257 - 1263
[4] Journal of the American Chemical Society, 1995, vol. 117, # 29, p. 7696 - 7710
[5] Tetrahedron, 2011, vol. 67, # 30, p. 5382 - 5388

TRIS(1-PYRROLIDINYL)PHOSPHINE 97 Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from TRIS(1-PYRROLIDINYL)PHOSPHINE 97 manufacturers

XINXIANG RUNYU MATERIAL CO., LTD.
Product
Tri(1-pyrrolidinyl)phosphine 5666-12-6
Price
US $0.00-0.00/Kg
Min. Order
1Kg
Purity
98%
Supply Ability
300Kg
Release date
2025-08-02

5666-12-6, TRIS(1-PYRROLIDINYL)PHOSPHINE 97Related Search:


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  • Tri(pyrrolidin-1-yl)phosphane
  • TRIS(1-PYRROLIDINYL)PHOSPHINE 97
  • Tris(N-pyrrolidinyl)phosphine
  • Tris(pyrrolidino)phosphine
  • Tripyrrolidinophosphine
  • TRIS(1-PYRROLIDINYL)PHOSPHINE 97%
  • phosphorous acid tripyrrolidide
  • Phosphorous acid tripyrrolidide, Tris(N,N-tetramethylene)phosphorous acid triamide
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  • Tripyrrolidinophsphine
  • Tripyrrolidine phosphine
  • 5666-12-6
  • C12H24N3P