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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894019Generated: October 31, 2026

2-Acetylamino-5-formyl-4-trifluoromethyl-benzoic acid methyl ester → 2-Acetylamino-5-(1-hydroxy-propyl)-4-trifluoromethyl-benzoic acid methyl ester

https://huagongshe.com/reaction/1894019

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Acetylamino-5-formyl-4-trifluoromethyl-benzoic acid methyl esterHCID 59164423—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
Product2-Acetylamino-5-(1-hydroxy-propyl)-4-trifluoromethyl-benzoic acid methyl esterHCID 5916445828.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2-acetylamino-5-formyl-4-trifluoromethyl-benzoic acid methyl ester (840 mg, 2.90 mmol) in dry diethyl ether (29 mL) was cooled to 0° C. and a solution of ethylmagnesium bromide (1M in THF, 5.8 mL, 5.8 mmol) was added dropwise. The mixture was stirred for 1 h at 0° C. and the reaction was quenched by adding aqueous ammonium chloride solution. This mixture was extracted once with EtOAc and the organic phase was then washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by flash chromatography (silica gel 60, hexanes/EtOAc 80:20→70:30) to furnish 2-acetylamino-5-(1-hydroxy-propyl)-4-trifluoromethyl-benzoic acid methyl ester (262 mg, 0.82 mmol, 28%) as a white solid, m.p. 120-122° C., ESI-MS: m/z 320 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513268B2
Source datasetuspto-grants-2013_08
ORD IDord-79f7c2606c2a4e13b05294628dce5009
Source noteuspto-grants-2013_08