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About This Item
Linear Formula:
C6H4[CH2P[C(CH3)2]2]
CAS Number:
Molecular Weight:
394.55
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.22
MDL number:
Product Name
1,2-Bis(di-tert-butylphosphinomethyl)benzene,
form
solid
Quality Level
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
functional group
phosphine
SMILES string
CC(C)(C)P(Cc1ccccc1CP(C(C)(C)C)C(C)(C)C)C(C)(C)C
InChI
1S/C24H44P2/c1-21(2,3)25(22(4,5)6)17-19-15-13-14-16-20(19)18-26(23(7,8)9)24(10,11)12/h13-16H,17-18H2,1-12H3
InChI key
SFCNPIUDAIFHRD-UHFFFAOYSA-N
General description
1,2-Bis(di-tert-butylphosphinomethyl)benzene (DTBPMB) is a bidentate phosphine ligand. DTBPMB in combination with Pd2(dba)3 (dba = trans,trans-dibenzylideneacetone) and a sulfonic acid can catalyze the methoxycarbonylation of ethane to form methyl propanoate.
Application
DTBPMB may be used as a ligand for the palladium-catalyzed hydroesterification of styrene and vinyl acetate to form branched esters in the presence of polymeric sulfonic acids promoters.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Highly active and selective catalysts for the production of methyl propanoate via the methoxycarbonylation of ethene.
Clegg W, et al.
Chemical Communications (Cambridge, England), 18, 1877-1878 (1999)
Highly active and selective palladium catalyst for hydroesterification of styrene and vinyl acetate promoted by polymeric sulfonic acids.
Ooka H, et al.
Chemical Communications (Cambridge, England), 9, 1173-1175 (2005)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 631922-1G | 04061826697856 |
| 631922-5G | 04061833366646 |