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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485718Generated: October 31, 2026

(2S)-2-hydroxy-2-(3-phenoxyphenyl)acetonitrile → HCID 131714315, compound

https://huagongshe.com/reaction/485718

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-2-hydroxy-2-(3-phenoxyphenyl)acetonitrileHCID 9837437—
ReactantHCID 131714316HCID 131714316—
SolventChloroformHCID 6212—
ProductHCID 131714315HCID 13171431579%

Reaction Steps

Using the procedure of Example 1, 0.6 g of the acid of Step C of Example 27 and 0.73 g of (S)α-cyano-3-phenoxy-benzyl alcohol were reacted to obtain 1.0 g of (S)α-cyano-3-phenoxybenzyl (1R,trans) 2,2-dimethyl-3-(3-chloro-1,2-propadienyl)cyclopropane-carboxylate with a specific rotation of [α]D20 =+26°±2° (c=0.75% in CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04537897
Source datasetuspto-grants-1985_08
ORD IDord-83268f83f19c4df899a708a398db909b
Source noteuspto-grants-1985_08