HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727249Generated: October 31, 2026
2,5-Dimethoxyaniline → N-(2,5-dimethoxyphenyl)cyclohexanecarboxamide
https://huagongshe.com/reaction/1727249
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,5-Dimethoxyaniline | HCID 7613 | — |
| Reactant | Cyclohexanecarbonyl chloride | HCID 75938 | — |
| Reactant | Ethylacetate heptane | HCID 21899848 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2,5-dimethoxyphenyl)cyclohexanecarboxamide | HCID 531821 | 80.5% |
Reaction Steps
1 ml (7.62 mmol, 1.1 eq.) of cyclohexanoic acid chloride is added to a solution of 1.05 g (6.89 mmol) of 2,5-dimethoxyaniline in 10 ml of a mixture toluene/methanol (1/1). The reaction mixture is maintained under stirring at 70° C. for 1.5 hour, and, after returning to ambient temperature, is poured into 50 ml of water. The expected product is extracted twice with 50 ml of toluene, then washed twice with 50 ml of water. The organic phases are combined, dried over magnesium sulphate and the solvent evaporated off under reduced pressure. 1.46 g (yield=67%) of N-(2,5-dimethoxyphenyl)cyclohexanecarboxamide is obtained and used without other purification in the following stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07495021B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-d26a9494e6684d67b39c5a48ac167add |
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| Source note | uspto-grants-2009_02 |
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