HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (2R)-3-methyl-2-{[4-(trifluoromethyl)phenyl]amino}butan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-[4-(trifluoromethyl)phenyl]-D-valine | HCID 13388455 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2R)-3-methyl-2-{[4-(trifluoromethyl)phenyl]amino}butan-1-ol | HCID 66968920 | 47% |
Reaction Steps
N-[4-(Trifluoromethyl)phenyl]-D-valine (2.15 g, 8.23 mmol) obtained in Step 1 of Example 1 was dissolved in tetrahydrofuran (50 ml), and triethylamine (1.71 mL, 12.3 mmol) and ethyl chloroformate (0.94 mL, 9.88 mmol) were added under cooling. The precipitated salt was filtered off, sodium borohydride (0.62 g, 16.4 mmol) and ice were added, and the mixture was stirred overnight at room temperature. The solvent was evaporated and, after work-up according to a conventional method, the residue was purified by silica gel column chromatography (30% mixed solvent of ethyl acetate/hexane) to give the title compound (0.95 g, 3.84 mmol, 47%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879863B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-b0d618ff56ef4c7cb7eadcdbbf86cff9 |
| Source note | uspto-grants-2011_02 |