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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719753Generated: October 26, 2026

(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2,2-trifluoroethoxy)-1-propenyl]-cyclopropane-carboxylic acid → (R)alpha-methyl-3-phenoxy-benzyl (1R,cis) 2,2-dimethyl-3-[(Z) 3-oxo-3-(2,2,2-trifluoroethoxy)-1-propenyl]-cyclopropane-carboxylate

https://huagongshe.com/reaction/1719753

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2,2-trifluoroethoxy)-1-propenyl]-cyclopropane-carboxylic acidHCID 13390085—
Reactant(1R)-1-(3-phenoxyphenyl)ethan-1-olHCID 22815813—
SolventChloroformHCID 6212—
Product(R)alpha-methyl-3-phenoxy-benzyl (1R,cis) 2,2-dimethyl-3-[(Z) 3-oxo-3-(2,2,2-trifluoroethoxy)-1-propenyl]-cyclopropane-carboxylateHCID 131714331—

Reaction Steps

Using the procedure of Step F of Example 9, the acid of Step D of Example 1 and (R)α-methyl-3-phenoxy-benzyl alcohol were reacted to obtain (R)α-methyl-3-phenoxy-benzyl (1R,cis) 2,2-dimethyl-3-[(Z) 3-oxo-3-(2,2,2-trifluoroethoxy)-1-propenyl]-cyclopropane-carboxylate with a specific rotation of [α]D20 =+108.5°±2° (c=1% in CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04542142
Source datasetuspto-grants-1985_09
ORD IDord-fbb6999e79c94ee2ac8bf554a3de7546
Source noteuspto-grants-1985_09