HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylethanolamine → (R)-(-)-2-Amino-1-phenylethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylethanolamine | HCID 1000 | — |
| Reactant | L-Tyrosine, N-(1,1-dimethylethoxy)carbonyl- | HCID 117439 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | (R)-(-)-2-Amino-1-phenylethanol | HCID 6951165 | 28% |
Reaction Steps
n-Butanol (20 ml) was added with the concentrate of the reaction products obtained in the same manner as in Example 296 which contained 1.67 g (7.50 mmol) of 2-amino-1-phenylethanol, and 2.11 g (7.50 mmol) of Boc-L-Tyr. The resultant mixture was heated for dissolution, cooled to room temperature and left over night to precipitate crystals. The crystals were isolated by filtration to afford 1.06 g (2.10 mmol) of (R)-2-amino-1-phenylethanol.Boc-L-Tyr salt. The yield of the compound based on (R)-2-amino-1-phenylethanol in the concentrate was 56.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06528686B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-eca69ceec9c748b48a5c69665c7f4050 |
| Source note | uspto-grants-2003_03 |