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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Phenethylamine, (+)- | HCID 643189 | — |
| Reactant | (2S)-2-(4-bromophenyl)oxirane | HCID 12163514 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | (S)-1-(4-Bromophenyl)-2-(((R)-1-phenylethyl)amino)ethan-1-ol | HCID 59317732 | 64.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106045B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-c7e0c74084ce4b748902db17c75b9781 |
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| Source note | uspto-grants-2012_01 |
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