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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099671Generated: October 30, 2026

Binap, (A+-)- → HCID 67278909, compound

https://huagongshe.com/reaction/2099671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBinap, (A+-)-HCID 634876—
ReactantHCID 57795502HCID 57795502—
ReactantHCID 57945297HCID 57945297—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67278909HCID 67278909—

Reaction Conditions

Temperature80 °C

Reaction Steps

Nitrogen was bubbled through a mixture of 2-triisopropylsilanyloxy-1-triisopropylsilanyloxymethyl-ethylamine (prepared from serinol using triisopropylsilyl chloride) (420 mg, 1.04 mmol) and 3-bromo-5-(4,4-dimethyl-cyclohex-1-enyl)-thiophene-2-carboxylic acid methyl ester (350 mg, 1.06 mmol) in dioxane (3.5 mL) containing CS2CO3 (1 g, 3.07 mmol) and Pd2(dba)3 (96 mg, 0.1 mmol) for 6 min. 2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl (105 mg, 0.17 mmol) was added and the mixture was stirred at 80° C. for 24 h. It was diluted with DCM, filtered through celite and evaporated. 5-(4,4-Dimethyl-cyclohex-1-enyl)-3-(2-triisopropylsilanyloxy-1-triisopropylsilanyloxymethyl-ethylamino)-thiophene-2-carboxylic acid methyl ester was obtained by chromatography over silica gel (hexane:EtOAc—95:5) (500 mg, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569600B2
Source datasetuspto-grants-2009_08
ORD IDord-1b13486f9c2b475a83829a3a6bda26e6
Source noteuspto-grants-2009_08