HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3496Generated: October 25, 2026
Water → Ethyl 4-[(2-methylbenzoyl)amino]benzoate
https://huagongshe.com/reaction/3496
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzocaine | HCID 2337 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methylbenzoyl chloride | HCID 70276 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-[(2-methylbenzoyl)amino]benzoate | HCID 689910 | 76.5% |
Reaction Steps
A mixture of 43.42 g of ethyl 4-aminobenzoate and 40.8 g of 2-methylbenzoyl chloride in 150 ml of dichloromethane is cooled in an ice bath and 26.56 g of triethylamine the solution is stirrer the addition, the solution is stirred at room temperature overnight. The mixture is poured into water and the organic layer separated. The organic layer is washed with water, 1N HCl, 1M NaHCO3 and dried over Na2SO4. The solvent is removed and the solid slurried with ethyl acetate and filtered to give 57 g of ethyl 4-[(2-methylbenzoyl)amino]benzoate as crystals, m.p. 110°-115° C. A mixture of 50.7 g of the preceding compound in 280 ml of ethyl alcohol and 55 ml of 10N NaOH is refluxed for 5 minutes. The mixture is cooled to room temperature, diluted with 200 ml of water and acidified with concentrated hydrochloric acid (pH 1-2). The mixture is filtered and the solid washed with water and dried to give 51 g of the desired product as white crystals, m.p. 270°-275° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05733905 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-487ac92980e343ec8d41d66e51566ec1 |
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| Source note | uspto-grants-1998_03 |
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