HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412035Generated: November 2, 2026
2-Ethoxybenzoyl chloride → 2-(2-Ethoxybenzamido)-6-methylbenzamide
https://huagongshe.com/reaction/412035
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Ethoxybenzoyl chloride | HCID 3016397 | — |
| Reactant | 2-Amino-6-methylbenzamide | HCID 16782469 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-(2-Ethoxybenzamido)-6-methylbenzamide | HCID 18536600 | — |
Reaction Steps
A mixture of 2-amino-6-methylbenzamide (UK Patent Application No 1,276,359; 5.49 g, 0.0365 mol), 2-ethoxybenzoyl chloride (7.67 g, 0.0415 mol) and pyridine (100 ml) was stirred at room temperature for 20 hours. The solvent was then removed by evaporation under vacuum and the residue dissolved in dichioromethane (200 ml). The solution was washed with saturated aqueous sodium carbonate solution (200 ml) and the aqueous phase back-extracted with further dichioromethane (2×100 ml). The organic solutions were combined, washed successively with 2N hydrochloric acid (3×100 ml) and brine (100 ml), then dried (Na2SO4) and evaporated under vacuum to give the title compound, which recrystallized from ethyl acetate as a colourless solid (6.86g, 63%), m.p. 166-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562830B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-a2e6d412084e47c1b525007a4f0d7365 |
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| Source note | uspto-grants-2003_05 |
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