HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2-Trifluoromethyl-thiazol-4-yl)ethylene oxide → N-[2-(4-Carbomethoxyphenyl)-1-methylethyl]-2-hydroxy-2-(2-trifluoromethyl-thiazol-4-yl)ethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2-Trifluoromethyl-thiazol-4-yl)ethylene oxide | HCID 14372861 | — |
| Reactant | Methyl 4-(2-aminopropyl)benzoate | HCID 15034329 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[2-(4-Carbomethoxyphenyl)-1-methylethyl]-2-hydroxy-2-(2-trifluoromethyl-thiazol-4-yl)ethanamine | HCID 19974173 | — |
Reaction Steps
0.54 g (0.030 mol) of 2-(2-trifluoromethyl-thiazol-4-yl)ethylene oxide is dissolved in 5 ml of ethanol, and the solution is added dropwise within 10 minutes to a boiling solution of 0.58 g (0.0030 mol) of 2-(4-carbomethoxyphenyl)-1-methylethylamine in 13 ml ethanol. The mixture is then boiled under reflux for 5 hours, the solvent is removed by distillation, and the base is purified on a silica gel column using methylene chloride/methanol=20:1 as eluant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04886814 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-7144da5320a74224990d241e06098fcd |
| Source note | uspto-grants-1989_12 |