HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991430Generated: November 2, 2026
Benzoic acid, 4-(acetyloxy)- → p-Acetoxybenzoyl chloride
https://huagongshe.com/reaction/991430
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoic acid, 4-(acetyloxy)- | HCID 16865 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | p-Acetoxybenzoyl chloride | HCID 2756254 | — |
Reaction Steps
Oxalyl chloride (0.35 ml) was added to a stirred suspension of 4-acetoxybenzoic acid (0.57 g) in methylene chloride (15 ml) which had been cooled to 0° C. DMF (2 drops) was added and the mixture was stirred at ambient temperature for 4 hours. The mixture was evaporated to give 4-acetoxybenzoyl chloride which was used without further purification. A mixture of the acid chloride so obtained, N-(3-amino-4-chlorophenyl)-4-cyanobenzamide (0.813 g) and pyridine (15 ml) was stirred and heated at 100° C. for 16 hours. The mixture was cooled to ambient temperature and poured into 2N aqueous hydrochloric acid solution (175 ml). The precipitate was isolated, washed with water and dried. The material so obtained was purified by column chromatography on silica using a 7:3 mixture of isohexane and ethyl acetate as eluent. There was thus obtained the title compound (0.74 g); m.p. 195-196° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06465455B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-bf438f129d634d4c9cb247d55e48924b |
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| Source note | uspto-grants-2002_10 |
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