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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844781Generated: November 1, 2026

Ammonia → 4-Ethynyl-3-nitrobenzamide

https://huagongshe.com/reaction/1844781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantMethyl 4-ethynyl-3-nitrobenzoateHCID 86694785—
SolventTetrahydrofuranHCID 8028—
Product4-Ethynyl-3-nitrobenzamideHCID 5696236653.2%

Reaction Steps

7.3 g (0.036 mol) Methyl 4-ethynyl-3-nitrobenzoate (Compound II-1), 300 ml methanol and 200 ml tetrahydrofuran were added into a reaction flask, stirred, and ammonia gas was passed through for 1 hour. Then the mixture was reacted at room temperature for 24 hours. After completion of the reaction monitored by TLC, the mixture was concentrated under reduced pressure with most of the tetrahydrofuran and methanol evaporated, then extracted with 300 ml ethyl acetate. The organic layer was washed with water for three times, dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated to dryness, and separated by column chromatography to obtain 4-ethynyl-3-nitrobenzamide (compound I-1), 3.6 g (0.0019 mol), yield 53.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946478B2
Source datasetuspto-grants-2015_02
ORD IDord-c829cf25f5a9463fa7b78dc4feee3ba8
Source noteuspto-grants-2015_02