Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569520Generated: October 30, 2026

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

https://huagongshe.com/reaction/569520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroethanolHCID 8259—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantTert.-butyl(1R,cis)2,2-dimethyl-3-(carboxy ethynyl)cyclopropane-carboxylateHCID 13093787—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Producttert.butyl(1R,cis)2,2-dimethyl-3-(2,2,2-trichloroethoxycarbonylethynyl)-cyclopropane-carboxylateHCID 1309379081.1%

Reaction Steps

6.2 g of dicyclohexylcarbodiimide were introduced into a solution of 7.15 g of tert.-butyl(1R,cis)2,2-dimethyl-3-(2-carboxyethynyl)-cyclopropane-carboxylate and 80 mg of 4-dimethylamino-pyridine in 35 ml of methylene chloride and the reaction mixture was stirred for 10 minutes after which 4.5 g of 2,2,2-trichloroethanol were added. The mixture was stirred for 1 hour and was filtered. The filtrate was washed with N hydrochloric acid, then with water until neutral, dried and evaporated to dryness. The 14 g of oil residue were chromatographed over silica gel and eluted with a 97-3 mixture of benzene-ethyl acetate to obtain 9 g of tert.butyl(1R,cis)2,2-dimethyl-3-(2,2,2-trichloroethoxycarbonylethynyl)-cyclopropane-carboxylate melting at 70°-71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04732903
Source datasetuspto-grants-1988_03
ORD IDord-8d5795f91a5d47759245c8790ba4d281
Source noteuspto-grants-1988_03