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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447920Generated: November 2, 2026

Pyridine → alpha-Cyano-m-phenoxybenzyl alpha-isopropyl-4-trifluoromethoxyphenylacetate

https://huagongshe.com/reaction/1447920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaS)-HCID 93218—
ReactantHCID 20343288HCID 20343288—
SolventDiethyl EtherHCID 3283—
Productalpha-Cyano-m-phenoxybenzyl alpha-isopropyl-4-trifluoromethoxyphenylacetateHCID 5421517439.5%

Reaction Steps

A solution of α-isopropyl-4-trifluoromethoxyphenylacetyl chloride (4.58 mmole) in ether (5 ml) is added to a ether (20 ml) solution of α-cyano-m-phenoxybenzyl alcohol (4.58 mmole) and pyridine (0.5 ml). The mixture is stirred overnight and filtered. The filtrate and the washings are evaporated and the residual oil is purified on 5×2 mm silica gel plates using 1:1 methylenechloride-hexane as eluent. The band with Rf=0.55 is extracted with ether and evaporated to give the desired ester (0.85 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04178460
Source datasetuspto-grants-1979_12
ORD IDord-e56c6bfe488548b2b0e4b3c578962db4
Source noteuspto-grants-1979_12