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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441527Generated: November 3, 2026

Acetic Anhydride → 2-Acetylamino-5-iodo-4-trifluoromethyl-benzoic acid methyl ester

https://huagongshe.com/reaction/1441527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 2-amino-5-iodo-4-(trifluoromethyl)benzoateHCID 53436880—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-Acetylamino-5-iodo-4-trifluoromethyl-benzoic acid methyl esterHCID 5916443392%

Reaction Steps

A solution of 2-amino-5-iodo-4-trifluoromethyl-benzoic acid methyl ester (42.0 g, 122 mmol) in toluene (400 mL) was treated with acetic anhydride (12.8 mL, 135 mmol) and the mixture was heated to reflux for 16 h under nitrogen. It was then allowed to cool to r.t. and diluted with water. The mixture was rendered neutral by adding small portions of sodium hydrogencarbonate, and the organic layer was separated. The aqueous phase was extracted with EtOAc, and the combined organic phases were dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product was recrystallized in hexanes to give 2-acetylamino-5-iodo-4-trifluoromethyl-benzoic acid methyl ester (43.4 g, 112 mmol, 92%) as a white powder, m.p. 96-98° C., ESI-MS: m/z 388 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655666B2
Source datasetuspto-grants-2010_02
ORD IDord-0732c87d09654ddba4e8745bcffb6952
Source noteuspto-grants-2010_02