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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424413Generated: October 29, 2026

1-Phenethylamine, (+)- → (S)-1-(4-Bromophenyl)-2-(((R)-1-phenylethyl)amino)ethan-1-ol

https://huagongshe.com/reaction/424413

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenethylamine, (+)-HCID 643189—
Reactant(2S)-2-(4-bromophenyl)oxiraneHCID 12163514—
SolventDiisopropyl EtherHCID 7914—
Product(S)-1-(4-Bromophenyl)-2-(((R)-1-phenylethyl)amino)ethan-1-olHCID 5931773264.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of (2S)-2-(4-bromophenyl)oxirane (55.0 g) and (R)-1-phenylethylamine (98.2g, 810 mmol) was heated at 80° C. for 6 hours. Addition of isopropyl ether (200 ml) to the residue after distillation of excess phenethylamine and successive filtration yielded (1S)-1-(4-bromophenyl)-2-((1R)-1-phenylethylamino)ethanol (57.0 g) as white crystals. Further crystallization was performed by the concentration of the filtrate in vacuo and cooling the residue in refrigerator. Filtration of the crystal with isopropyl ether (30 ml) yielded additional title compound (5.60 g) as crystals (72.4% yield, 3 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106045B2
Source datasetuspto-grants-2012_01
ORD IDord-c7e0c74084ce4b748902db17c75b9781
Source noteuspto-grants-2012_01