HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Methoxybenzylamine → HCID 57754052, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Methoxybenzylamine | HCID 21156 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Trifluoromethanesulfonic acid, lithium salt | HCID 3664839 | — |
| Reactant | (1R,2S)-[2-(3,4-difluoro-phenyl)-1-oxiranyl-ethyl]-carbamic acid tert-butyl ester | HCID 86616462 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57754052 | HCID 57754052 | — |
Reaction Steps
A solution of (1R,2S)-[2-(3,4-difluoro-phenyl)-1-oxiranyl-ethyl]-carbamic acid tert-butyl ester (0.03 g, 0.1 mmol) in acetonitrile (1 mL) was treated with lithium triflate (0.032 g, 0.2 mmol) and stirred at ambient temperature for 20 minutes. Then 3-methoxybenzylamine (0.016 mL, 0.12 mmol) was added to the reaction neat in one portion. The reaction was stirred at ambient temperature for 14 hours. The reaction was poured into saturated ammonium chloride solution (5 mL), extracted with ethyl acetate, the organic phase separated, dried (MgSO4) and the solvent removed at reduced pressure. The product was obtained as an oil and used without further purification (0.041 g, 94%). MS: 437 (M+H, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07557137B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-102b0fd138274c048ebe5de232edecef |
| Source note | uspto-grants-2009_07 |