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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102805Generated: October 30, 2026

Water → Benzamide

https://huagongshe.com/reaction/2102805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl chlorideHCID 7412—
Reactant2-Amino-6-nitrobenzothiazoleHCID 22704—
SolventPyridineHCID 1049—
ProductBenzamideHCID 233186%

Reaction Steps

To a suspension of 2-amino-6-nitrobenzothiazole (Sigma Aldrich, 2.93 g, 15 mmol) in pyridine (20 mL), benzoyl chloride (1.74 mL, 15 mmol) was added. After stirring over-night at r.t., additional benzoyl chloride (1.74 mL, 15 mmol) was added and the mixture was stirred at 60° C. After completion of the reaction, the mixture was poured into water (250 mL) and stirred overnight at r.t. Separation of the resulting precipitate yielded N-6-nitrobenzotihiazol-2-yl)benzamide (3.87 g, 12.9 mmol, 86%) as a yellow solid. LC/ESI-MS: m/z=300 [M+H]+; m/z=298 [M−H]−; Rt=3.93 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576090B2
Source datasetuspto-grants-2009_08
ORD IDord-c11eb08136cd4546907c236f1cce103d
Source noteuspto-grants-2009_08