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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860320Generated: October 31, 2026

Phenylethanolamine → (R)-(-)-2-Amino-1-phenylethanol

https://huagongshe.com/reaction/1860320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylethanolamineHCID 1000—
ReactantL-Tyrosine, N-(1,1-dimethylethoxy)carbonyl-HCID 117439—
Solvent1-ButanolHCID 263—
Product(R)-(-)-2-Amino-1-phenylethanolHCID 695116528%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528686B1
Source datasetuspto-grants-2003_03
ORD IDord-eca69ceec9c748b48a5c69665c7f4050
Source noteuspto-grants-2003_03