Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 68294666 | HCID 68294666 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68294110 | HCID 68294110 | 96.4% |
Reaction Steps
To a solution of 282 (0.5 g, 2.1 mmol) and THF (10 mL) was added BH3—SMe2 (2.1 mL, 4.3 mmol) and the reaction was stirred at 65° C. for 8 h. The reaction was poured into water and extracted with DCM. The combined organic extracts were dried (MgSO4), filtered, and concentrated in vacuo. The crude product was purified by SiO2 chromatography eluting with EtOAc/MeOH/NH4OH (90/9/1) to afford 0.48 g (94%) of (S)-3-amino-1-(3-fluoro-4-(trifluoromethyl)phenyl)propan-1-ol (284).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133187B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-6947094ee6384731a990d422d023b767 |
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| Source note | uspto-grants-2015_09 |
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