HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Dimethoxybenzoyl chloride → N-[5-(1-Ethylcyclohexyl)-1,2-oxazol-3-yl]-2,6-dimethoxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Dimethoxybenzoyl chloride | HCID 74810 | — |
| Reactant | 5-(1-Ethylcyclohexyl)-1,2-oxazol-3-amine | HCID 13234262 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[5-(1-Ethylcyclohexyl)-1,2-oxazol-3-yl]-2,6-dimethoxybenzamide | HCID 13234271 | 60.2% |
Reaction Steps
A solution of 14 g of 3-amino-5-(1-ethylcyclohexyl)isoxazole and 14.4 g of 2,6-dimethoxybenzoyl chloride in 100 ml of toluene was heated to reflux and stirred for eighteen hours. The reaction mixture then was cooled to room temperature and the solvent was removed by evaporation under reduced pressure to provide a solid. The solid was dissolved in 200 ml of dichloromethane, washed with dilute sodium hydroxide and with brine, dried, and the solvent was removed by evaporation. The product was crystallized from dichloromethane and diethyl ether to provide 15.5 g of N-[5-(1-ethylcyclohexyl)-3-isoxazolyl]-2,6-dimethoxybenzamide. M.P. 179°-181° C. Yield 60%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04636243 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-ddb667917b4b466d9a7b635ae9e6c009 |
| Source note | uspto-grants-1987_01 |