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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenethylamine, (+)-HCID 643189—
Reactant(+)-3-Acetoxy-2-(4-bromophenyl)propyl 4-methyl-benzenesulfonateHCID 86664263—
SolventDimethylformamideHCID 6228—
Product3-((R)-1-phenylethylamino)-2-(4-bromophenyl)propyl acetateHCID 6728244340.5%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108957B2
Source datasetuspto-grants-2015_08
ORD IDord-b8fa535c556c475e929aa647f6c86e06
Source noteuspto-grants-2015_08