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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14458Generated: October 25, 2026

Triethylamine → HCID 68703339, compound

https://huagongshe.com/reaction/14458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyryl chlorideHCID 62325—
Reactant2-(4-Chlorophenyl)-1-(3,4-difluoro-2-hydroxy-phenyl)-ethanoneHCID 68698513—
SolventDichloromethaneHCID 6344—
ProductHCID 68703339HCID 68703339—

Reaction Steps

A solution of 2-(4-chlorophenyl)-1-(3,4-difluoro-2-hydroxy-phenyl)-ethanone (4.5 g, 87% pure, 13.85 mmol) and triethylamine (1.7 g, 2.35 ml, 16.8 mmol, 1.2 eq.) in methylene chloride (100 ml) is treated dropwise at ambient temperature with isobutyryl chloride (1.79 g, 1.76 ml, 16.8 mmol, 1.2 eq.). After stirring for 5 h, the solution is washed successively with 2M HCl solution and saturated sodium hydrogen carbonate solution. The organic phase is dried over anhydrous magnesium sulphate, filtered and evaporated to dryness in vacuo to afford a black residue. This is triturated with methanol at room temperature overnight to afford a brown solid, which is filtered and washed with methanol. The solid is purified twice by flash chromatography (ethyl acetate/cyclohexane=1:9) to furnish the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732435B2
Source datasetuspto-grants-2010_06
ORD IDord-1a5857e3db8c41c8b57535852103d956
Source noteuspto-grants-2010_06