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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 70363152 | HCID 70363152 | — |
| Solvent | Nitric Acid | HCID 944 | — |
| Product | N-(4-bromo-2-nitrophenyl)acetamide | HCID 136690 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04914177 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-4c826a4887844833bf8dbe16506cc7dc |
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| Source note | uspto-grants-1990_04 |
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