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693049

Sigma-Aldrich

(R)-Tol-BINAP

Synonym(s):
(R)-(+)-2,2′-Bis(di-p-tolylphosphino)-1,1′-binaphthyl
Empirical Formula (Hill Notation):
C48H40P2
CAS Number:
Molecular Weight:
678.78
MDL number:
PubChem Substance ID:
NACRES:
NA.22

form

solid

Quality Level

optical activity

[α]20/D +162°, c = 0.5 in benzene

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
reaction type: Cross Couplings

mp

254-258 °C

functional group

phosphine

SMILES string

Cc1ccc(cc1)P(c2ccc(C)cc2)c3ccc4ccccc4c3-c5c(ccc6ccccc56)P(c7ccc(C)cc7)c8ccc(C)cc8

InChI

1S/C48H40P2/c1-33-13-23-39(24-14-33)49(40-25-15-34(2)16-26-40)45-31-21-37-9-5-7-11-43(37)47(45)48-44-12-8-6-10-38(44)22-32-46(48)50(41-27-17-35(3)18-28-41)42-29-19-36(4)20-30-42/h5-32H,1-4H3

InChI key

IOPQYDKQISFMJI-UHFFFAOYSA-N

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(R)-Tol-BINAP

Sigma-Aldrich

693049

(R)-Tol-BINAP

(S)-T-BINAP

Sigma-Aldrich

693030

(S)-T-BINAP

(R)-DM-BINAP

Sigma-Aldrich

692379

(R)-DM-BINAP

(R,R)-BABIBOP ≥97%

Sigma-Aldrich

912964

(R,R)-BABIBOP

form

solid

form

solid

form

solid

form

powder

optical activity

[α]20/D +162°, c = 0.5 in benzene

optical activity

[α]20/D -156°, c = 0.5 in benzene

optical activity

[α]20/D +169°, c = 1 in chloroform

optical activity

-

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: catalyst
reaction type: Cross Couplings

reaction suitability

-

reaction suitability

-

reaction suitability

-

mp

254-258 °C

mp

250-255 °C

mp

187-191 °C

mp

-

functional group

phosphine

functional group

-

functional group

-

functional group

-

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

General description

BINAP is based on a bis naphthalene backbone with different phosphine derivatives. 2,2′-bis(di-p-tolylphosphino)-1,1′-binaphthyl (p-Tol-BINAP)·AgF complex catalyzed asymmetric Mukaiyama-type aldol reaction is reported.

Application

(R)-T-BINAP complexes derived from rhodium precursors are used for the asymmetric hydroformylation of vinyl acetate. It may be employed as chiral catalyst for allylation of N-tosyl α-imino esters.
Catalyst involved in studies of the role of excess phosphine ligand in enantioselective conjugate addition of ethylmagnesium bromide and α,β-unsaturated ester

Reactant serving as a precursor for:
  • Catalysts used for reductive amination of ketones
  • Rh(I)-catalyst for hydrogenation of acetamidoacrylic acid derivatives
  • Chiral platinum catalysts for asymmetric Baeyer-Villiger oxidation of cyclic ketones
  • CuI-Tol-BINAP catalysts for enantioselective Michael reactions of Grignard reagents to unsaturated esters
  • BINAP Pt Dications for cation trapping

Legal Information

Sold in collaboration with Takasago for research purposes only.

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis

Enter Lot Number to search for Certificate of Analysis (COA).

Certificate of Origin

Enter Lot Number to search for Certificate of Origin (COO).

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