HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Benzenemethanamine, N-ethyl-4-(trifluoromethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Reactant | N-[4-(trifluoromethyl)benzyl]acetamide | HCID 23132710 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzenemethanamine, N-ethyl-4-(trifluoromethyl)- | HCID 485421 | 28% |
Reaction Steps
N-[4-(trifluoromethyl)benzyl]acetamide (3.085 g, 14.204 mmol) was dissolved in THF (100 ml) and was cooled to zero degrees under argon atmosphere. (Methylthio)methane compound with borane (1:1) (2.698 g, 35.511 mmol) was added and the mixture was refluxed over night at RT. HCl (15 ml, 10%) was gently added and was stirred overnight. The solvent was removed by evaporation Diethyl ether (20 ml) was added and the product was extracted to the water phase by K2CO3 (3×15 ml), the water phase was acidified by HCl (10 ml, 10%) and the product was extracted to the organic phase by EtOAc (3×15 ml). The organic phase was dried (MgSO4) and the solvent was removed by evaporation to give 0.809 g of N-[4-(trifluoromethyl)benzyl]ethanamine (yield 28%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351858B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-29b878b89e1047aca938bc0962bff8ca |
| Source note | uspto-grants-2008_04 |