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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27933Generated: October 25, 2026

Triethylamine → 4-Fluoro-3-phenoxybenzyl 2-(5-chloro-2-benzothienyl)-3-methylbutanoate

https://huagongshe.com/reaction/27933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(4-Fluoro-3-phenoxyphenyl)methanolHCID 12874224—
Reactant2-(5-Chloro-2-benzothienyl)-3-methylbutanoic acidHCID 54204673—
SolventDiethyl EtherHCID 3283—
Product4-Fluoro-3-phenoxybenzyl 2-(5-chloro-2-benzothienyl)-3-methylbutanoateHCID 54113473—

Reaction Steps

To a stirred solution of 4-fluoro-3-phenoxybenzyl alcohol (0.22 g, 0.99 mmol) and triethylamine (0.14 g, 1.38 mmol) in ether (about 15 ml), under nitrogen, is added by syringe a solution of the acid chloride of 2-(5-chloro-2-benzothienyl)-3-methylbutanoic acid (1.5 mmol) in ether. The mixture is stirred for about 1 hour and then quenched with saturated aqueous sodium bicarbonate. The ether phase is washed with aqueous sodium bicarbonate, water and brine and filtered through silica. Evaporation of solvent, followed by thin layer chromatography, gives 4-fluoro-3-phenoxybenzyl 2-(5-chloro-2-benzothienyl)-3-methylbutanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04224330
Source datasetuspto-grants-1980_09
ORD IDord-898488c243e84b2bad3076dfea519478
Source noteuspto-grants-1980_09