Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072745Generated: October 31, 2026

Acetic Anhydride → N-(4-bromo-2-nitrophenyl)acetamide

https://huagongshe.com/reaction/2072745

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 70363152HCID 70363152—
SolventNitric AcidHCID 944—
ProductN-(4-bromo-2-nitrophenyl)acetamideHCID 136690—

Reaction Conditions

Temperature65 °C

Reaction Steps

Preparation of 4-bromo-2-nitroaniline-4-bromoaniline (51.6 grams) and acetic anhydride (210 ml) were mixed under strong agitation. The temperature is raised to 65° C. in 10 minutes and slowly decreased to room temperature in one hour. An ice bath is used to maintain the temperature between 15°-20° C. and nitric acid (density 1.42, 30 ml) was added drop by drop in one hour. A yellow 4-bromo-2-nitroacetanilide was isolated by pouring the acetic anhydride solution into ice water followed by filtration. Hydrolysis of the acid acetanilide in aqueous hydrochloric acid (100 ml of concentrated HCL and 500 ml of water) at reflux temperatures for three hours yielded a 57% yield of 4-bromo-2-nitroaniline having the melting point of 109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914177
Source datasetuspto-grants-1990_04
ORD IDord-4c826a4887844833bf8dbe16506cc7dc
Source noteuspto-grants-1990_04