Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | alpha-Methyl-D-phenylalanine | HCID 7023409 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14919271 | HCID 14919271 | — |
Reaction Steps
To a solution of alpha-methyl-D-phenylalanine (1.74 g, 9.71 mmol) in 30 mL THF at rt was added NaBH4 (0.92 g 24.27 mmol) in one portion. The solution was cooled to 0° C. Iodine (2.46 g, 9.71 mmol) in 5 mL THF was added dropwise over 30 min. After the addition was complete, the reaction was heated to reflux for 2 days. The reaction was then cooled to 0° C. and quenched by the addition of methanol until the bubbling subsided. The reaction mixture was acidified by the addition of 6N HCl until pH 1, stirred at 50° C. for 30 min and concentrated in vacuo. Purification using ion exchange chromatography (SCX cartridge) afforded (R)-2-amino-2-methyl-3-phenylpropan-1-ol as a white solid. 1H NMR (400 MHz, CDCl3) δ 7.35-7.18 (m, 5H), 3.36 (A of AB, d, J=10.4 Hz, 1H), 3.31 (B of AB, d, J=10.4 Hz, 1H), 2.70 (s, 2H), 1.04 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07847100B2 |
|---|
| Source dataset | uspto-grants-2010_12 |
|---|
| ORD ID | ord-9c9ce02402b741a79f2953c9264513bf |
|---|
| Source note | uspto-grants-2010_12 |
|---|