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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906516Generated: October 30, 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/906516

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 numberUS08012988B2
Source datasetuspto-grants-2011_09
ORD IDord-b3422f9cb22b46b8a2cdb111e6cd9286
Source noteuspto-grants-2011_09