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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844786Generated: October 30, 2026

Acetic Anhydride → N-acetyl-4-ethynyl-3-nitrobenzamide

https://huagongshe.com/reaction/1844786

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Ethynyl-3-nitrobenzamideHCID 56962366—
SolventAcetic AcidHCID 176—
ProductN-acetyl-4-ethynyl-3-nitrobenzamideHCID 5733145322.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

4 g (0.021 mol) 4-Ethynyl-3-nitrobenzamide (Compound I-1), 30 ml (0.320 mol) acetic anhydride and 20 ml acetic acid were added into a reaction flask, stirred, and heated to 120° C. for 15 hours. After completion of the reaction monitored by TLC, the mixture was extracted with 300 ml ethyl acetate, and the organic layer was washed with water for three times, dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated to dryness, separated by column chromatography to obtain N-acetyl-4-ethynyl-3-nitrobenzamide (Compound I-11), 1.1 g (0.0047 mol), yield 22.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946478B2
Source datasetuspto-grants-2015_02
ORD IDord-7fd2ef2c5f17443797f467f183cc894c
Source noteuspto-grants-2015_02