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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719748Generated: October 25, 2026

Benzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaR)- → (R)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-difluoroethoxy)-1-propenyl]-cyclopropane-carboxylate

https://huagongshe.com/reaction/1719748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaR)-HCID 156232—
Reactant(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-difluoroethoxy)-1-propenyl]cyclopropane-carboxylic acidHCID 86740318—
SolventChloroformHCID 6212—
Product(R)alpha-cyano-3-phenoxy-benzyl(1R,cis)2,2-dimethyl-3-[(Z)3-oxo-3-(2,2-difluoroethoxy)-1-propenyl]-cyclopropane-carboxylateHCID 86740317—

Reaction Steps

Using the procedure of Step F of Example 9, (1R,cis) 2,2-dimethyl-3-[(Z) 3-oxo-3-(2,2-difluoroethoxy)-1 propenyl]-cyclopropane-carboxylic acid and (R)α-cyano-3-phenoxy-benzyl alcohol were reacted to obtain (R)α-cyano-3-phenoxy-benzyl (1R,cis) 2,2-dimethyl-3-[(Z) 3-oxo-3-(2,2-difluoroethoxy)-1-propenyl]-cyclopropane-carboxylate with a specific rotation of [α]D20 =+117.5°±3° (c=0.6% in chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04542142
Source datasetuspto-grants-1985_09
ORD IDord-2bcbeb4a713b4263bc3201dcd949eb98
Source noteuspto-grants-1985_09