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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114422Generated: October 30, 2026

Methylamine → [(1R)-1-(4-bromophenyl)-2-(4-morpholinyl)ethyl]methylamine

https://huagongshe.com/reaction/2114422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant4-[(2R)-2-(4-bromophenyl)-2-chloroethyl]morpholineHCID 59809618—
SolventEthanolHCID 702—
Product[(1R)-1-(4-bromophenyl)-2-(4-morpholinyl)ethyl]methylamineHCID 5742554293%

Reaction Conditions

Temperature0 °C

Reaction Steps

Crude 4-[(2R)-2-(4-Bromophenyl)-2-chloroethyl]morpholine (34.5 g) was dissolved in 200 mL of EtOH at room temperature with magnetic stirring. The resulting solution was cooled to 0° C. and treated with 71 ml of MeNH2 (33 wt % in EtOH) under N2. The reaction flask was capped by a rubber septum, and the reaction mixture was maintained at room temperature for 48 h. The reaction mixture was concentrated, and the residue was partitioned between EtOAc and sat NaHCO3(aq). The organic layer was washed by brine, dried over MgSO4, and filtered. The filtrate was concentrated to yield the title compound as a yellow solid (31.6 g, 93%). MS (ES) m/e 300, 301 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432258B2
Source datasetuspto-grants-2008_10
ORD IDord-3f272ee4ab184aed9e94610b4580981f
Source noteuspto-grants-2008_10