HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515460Generated: October 30, 2026
1-Phenethylamine, (+)- → 3-((R)-1-phenylethylamino)-2-(4-bromophenyl)propyl acetate
https://huagongshe.com/reaction/515460
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Phenethylamine, (+)- | HCID 643189 | — |
| Reactant | (+)-3-Acetoxy-2-(4-bromophenyl)propyl 4-methyl-benzenesulfonate | HCID 86664263 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-((R)-1-phenylethylamino)-2-(4-bromophenyl)propyl acetate | HCID 67282443 | 40.5% |
Reaction Steps
To a solution of (+)-3-acetoxy-2-(4-bromophenyl)propyl 4-methylbenzene-sulfonate (8.00 g, 18.7 mmol) in N,N-dimethylformamide (94.0 ml) was added (R)-(+)-1-phenylethylamine(11.3 g, 93.2 mmol) at room temperature. The mixture was stirred at 120° C. for 7 hours and concentrated in vacuo. The residue was partitioned between water and ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography (eluant: hexane/ethyl acetate=7/3) to afford diastereopure 3-((R)-1-phenylethylamino)-2-(4-bromophenyl)propyl acetate as pale yellow oil (2.85 g, 40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108957B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-b8fa535c556c475e929aa647f6c86e06 |
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| Source note | uspto-grants-2015_08 |
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