HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → 2-Amino-2-(3-bromophenyl)propan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Amino-2-(3-bromophenyl)propanoic acid hydrochloride | HCID 22336992 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Amino-2-(3-bromophenyl)propan-1-ol | HCID 53256694 | — |
Reaction Steps
NaBH4 (38 g, 1.125 mol) was added at room temperature to a slurry of 2-amino-2-(3-bromo-phenyl)-propionic acid hydrochloride (105 g, 375 mmol) in dry THF. At 0° C. BF3—O(C2H5)2 (158 g, 1.125 mol) was added dropwise. The mixture was allowed to warm to room temperature, stirred for three days, quenched with 1M aqueous NaOH solution, concentrated in vacuo to remove the THF and extracted with EtOAc (3×300 ml). The organic phase was washed with 1M aqueous NaOH solution, dried with sodium sulfate and concentrated in vacuo to yield the title compound, which was used in the next reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09284284B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-c561545baadd405fa4c5db447500330b |
| Source note | uspto-grants-2016_03 |