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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154416Generated: October 31, 2026

(2S)-2-hydroxy-2-(3-phenoxyphenyl)acetonitrile → HCID 86739822, compound

https://huagongshe.com/reaction/1154416

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-2-hydroxy-2-(3-phenoxyphenyl)acetonitrileHCID 9837437—
ReactantHCID 86739823HCID 86739823—
SolventChloroformHCID 6212—
ProductHCID 86739822HCID 86739822—

Reaction Steps

Using the process of Example 1, (1R,cis) 2,2-dimethyl-3(Z)-[2-bromo-3-oxo-3-tert.-butoxy-propenyl]-cyclopropane-1-carboxylic acid and (S)α-cyano-3-phenoxy-benzyl alcohol were reacted to obtain (S)α-cyano-3-phenoxy-benzyl (1R,cis) 2,2-dimethyl-3(Z)-[2-bromo-3-oxo-3-tert.-butoxy-propenyl]-cyclopropane-1-carboxylate with a specific rotation of [α]D20 =+16.5°±2° (c=0.5% in chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04489093
Source datasetuspto-grants-1984_12
ORD IDord-fcb66ab7eaed4ba2bf9acc5521e285fa
Source noteuspto-grants-1984_12