Basic information Reaction Safety Supplier Related
ChemicalBook >  Product Catalog >  Catalyst and Auxiliary >  (R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline

(R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline

Basic information Reaction Safety Supplier Related

(R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline Basic information

Product Name:
(R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline
Synonyms:
  • (R) QuinoxP
  • 2,3-Bis((R)-tert-butyl(methyl)phosphino)quinoxaline
  • (R,R)-(-)-2,3-Bis(tert-butylmethylphosphino)quinoxaline 97%
  • (R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline
  • (R,R)-QuinoxP*
  • (R) QuinoxP(R)
  • (R,R)-(-)-2,3-Bis(tert-butylmethylphosphino)quinoxaline
  • (R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline, min. 98% (R,R)-QuinoxP*
CAS:
866081-62-1
MF:
C18H28N2P2
MW:
334.38
Product Categories:
  • organophosphine ligand
Mol File:
866081-62-1.mol
More
Less

(R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline Chemical Properties

Melting point:
100-104 °C
alpha 
-54.3° (c 1.0, CHCl3)
Boiling point:
447.6±45.0 °C(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
Powder
pka
-0.54±0.59(Predicted)
color 
orange
InChIKey
DRZBLHZZDMCPGX-UHFFFAOYSA-N
More
Less

Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36/37/38
Safety Statements 
26
RIDADR 
UN2811 6.1/PG 3
WGK Germany 
3
HS Code 
2933.99.8290
More
Less

(R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline Usage And Synthesis

Reaction

  1. Ligand for the rhodium-catalyzed, asymmetric hydrogenation of dehydroamino acid esters and α-enamides.
  2. Ligand for the rhodium-catalyzed, asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated carbonyl compounds.
  3. Ligand for the rhodium-catalyzed, asymmetric alkylative ring opening reaction
  4. Ligand for the palladium-catalyzed asymmetric allylic alkylation and amination of racemic substrates.
  5. Ligand for the ruthenium-catalyzed asymmetric hydrogenation of ketones.
  6. Ligand for the rhodium-catalyzed, asymmetric hydroacylation of 1,1-disubstituted alkenes with aldehydes.
  7. Ligand for the silver-catalyzed asymmetric nitroso aldol reaction.
  8. Cu-catalyzed enantioconvergent allyllic borylation.
  9. Cu-catalyzed enantioselective cyclopropylation.


Description

(R,R)-(-)-2,3-Bis(tert-butylmethylphosphino)quinoxaline is an efficient ligand exhibiting high levels of enantiocontrol in synthetic transformations ranging from metal-catalyzed 1,4-addition of arylboronic acids to asymmetric hydrogenation to alkylative ring opening.

Uses

Air-Stable and Highly Efficient Chiral Ligands

Application

Air-Stable and Highly Efficient Chiral Ligands,Efficient ligand exhibiting high levels of enantiocontrol in synthetic transformations ranging from metal-catalyzed 1,4-addition of arylboronic acids to alkylative ring opening to asymmetric hydrogenation.

General Description

(R,R)-(-)-2,3-Bis(tert-butylmethylphosphino)quinoxaline is an air-stable C2-symmetric P-stereogenic phosphine ligand.

Synthesis


In 4 ml of tetrahydrofuran was dissolved 236 mg (2.0 mmol) of (R)-tert-butylmethylphosphine-borane (9), and the resulting solution was cooled to -78° C. with liquid nitrogen. To the cooled solution was added dropwise 1.25 ml of a 1.6 M hexane solution of n-butyllithium. Fifteen minutes later, a solution of 133 mg (0.67 mmol) of 2,3-dichloroquinoxaline (10) in 4 ml of tetrahydrofuran was added thereto dropwise while vigorously stirring to form a diphosphine-borane compound (11) as an intermediate. The liquid temperature was raised to room temperature over one hour, at which the mixture was stirred for 3 hours. One milliliter of TMEDA was added thereto, and the stirring was continued for an additional 2 hour period to complete deboranation. The reaction was ceased by addition of 1M hydrochloric acid. The reaction mixture was extracted with hexane. The extract was washed successively with 1M hydrochloric acid and a saturated sodium chloride aqueous solution and dried over sodium sulfate. The solvent was removed by evacuation, and the residue was purified by silica gel column chromatography (mobile phase: hexane/ethyl acetate=30/1) to give (R,R)-2,3-bis(tert-butylmethylphosphino)quinoxaline (12) as an orange solid. Recrystallization from 1.7 ml of hot methanol gave orange crystals (>99% ee) in a yield of 80%.

(R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxalineSupplier

Sphinx Scientific Laboratory(Tianjin) Co.,Ltd Gold
Tel
022-66211289808-808 13672102692
Email
contact@sphinxpharm.com
ChemicalRIM Co., Ltd Gold
Tel
15184345951
Email
chemicalRIM@gmail.com
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Email
jkinfo@jkchemical.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Beijing Ouhe Technology Co., Ltd
Tel
010-82967028 13552068683
Email
2355560935@qq.com
More
Less

(R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline(866081-62-1)Related Product Information