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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916482Generated: October 30, 2026

Nitric Acid → N-(2-bromo-6-nitrophenyl)acetamide

https://huagongshe.com/reaction/1916482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantAcetic AnhydrideHCID 7918—
Reactant2-BromoanilineHCID 11992—
ProductN-(2-bromo-6-nitrophenyl)acetamideHCID 464306216.7%

Reaction Steps

To a solution of 2-bromoaniline (XC) (50 g, 0.29 mol, 1 eq) in acetic anhydride (265 mL) was added dropwise nitric acid (fuming) (36.75 mL, 0.93 mol, 3.2 eq) at 0° C. and then stirred at that temperature, when the starting material was consumed, the mixture was filtered, the filtrate was poured into ice water. The aqueous phase was basified with aqueous solution of sodium bicarbonate to pH=7, then the mixture was extracted with EtOAc (30 mL×3). The organic layers were combined, dried and concentrated in vacuo to give the N-(2-bromo-6-nitrophenyl)acetamide (XCI) (12.6 g, 48.6 mmol, 16.7% yield) as a white solid. 1H NMR (DMSO-d6, 400 MHz) δ ppm 2.06 (s, 3H), 7.43 (t, J=8 Hz, 1H), 7.94 (d, J=8 Hz, 1H), 8.05 (d, J=8 Hz, 1H); ESIMS found for C8H7BrN2O3 m/z 259 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618128B1
Source datasetuspto-grants-2013_12
ORD IDord-b2afec0b5ee04ace8f06c286afd4a12f
Source noteuspto-grants-2013_12