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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464450Generated: October 30, 2026

Trichloroethanol → tert.butyl(1R,cis)2,2-dimethyl-3-(2,2,2-trichloroethoxycarbonylethynyl)-cyclopropane-carboxylate

https://huagongshe.com/reaction/464450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroethanolHCID 8259—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantTert.-butyl(1R,cis)2,2-dimethyl-3-(carboxy ethynyl)cyclopropane-carboxylateHCID 13093787—
Catalyst2-DimethylaminopyridineHCID 21885—
SolventDichloromethaneHCID 6344—
Producttert.butyl(1R,cis)2,2-dimethyl-3-(2,2,2-trichloroethoxycarbonylethynyl)-cyclopropane-carboxylateHCID 1309379081.1%

Reaction Steps

A mixture of 6.2 g of dicyclohexylcarbodiimide, 7.15 g of tert.-butyl(1R,cis)2,2-dimethyl-3-(2-carboxyethynyl)-cyclopropane-carboxylate, 80 mg of dimethylaminopyridine and 35 ml of methylene chloride was stirred for 10 minutes and 4.5 g of 2,2,2-trichloroethanol were added thereto. The mixture was stirred for one hour and was filtered and the filtrate was washed with N hydrochloric acid and then with water until the wash water was neutral, dried and evaporated to dryness. The 14 g of oil residue were chromatographed over silica gel and eluted with a 97-3 benzeneethyl acetate mixture to obtain 9 g of tert.-butyl(1R,cis)2,2-dimethyl-3-[2,2,2-trichloroethoxycarbonyl-ethynyl]-cyclopropane-carboxylate melting at 70°-71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04547522
Source datasetuspto-grants-1985_10
ORD IDord-47acb165439743e5bbb4b44331bcbf19
Source noteuspto-grants-1985_10