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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603613Generated: October 26, 2026

Acetic Anhydride → N-(3-bromo-5-nitrophenyl)acetamide

https://huagongshe.com/reaction/1603613

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactantar-Bromo-ar-nitrobenzenamineHCID 44535—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductN-(3-bromo-5-nitrophenyl)acetamideHCID 1065890891.5%

Reaction Steps

28.40 g (0.131 mol) of 3-bromo-5-nitroaniline were dissolved in 250 ml of pyridine and treated with 30 ml (0.317 mol) of acetic anhydride. The mixture was stirred at room temperature for 18 hrs. and subsequently at 40° C. for 2 hrs. Then, the residue was digested in water and the precipitate was filtered off. The filter material was rinsed with a large amount of water and dried at 45° C. in a high vacuum. There were obtained 31.0 g (91.5%) of N-(3-bromo-5-nitrophenyl)-acetamide as orange-yellow crystals. MS (ISP): me/e=260, 258 (C8H8BrN2O3+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05990105
Source datasetuspto-grants-1999_11
ORD IDord-849c30a95b584c4cb3098744679e5144
Source noteuspto-grants-1999_11