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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114417Generated: October 31, 2026

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

https://huagongshe.com/reaction/2114417

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 MeNH2 (71 mL, 33 wt % in EtOH) under N2. The reaction flask was capped with a rubber septum and the reaction mixture maintained at room temperature for 48 h. The mixture was then concentrated and the residue was partitioned between EtOAc and saturated aqueous NaHCO3. The organic layer was washed with brine, dried over MgSO4, and filtered. The filtrate was concentrated to yield the title compound as a yellow solid (32 g, 93%). MS (ES) m/e 300 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432258B2
Source datasetuspto-grants-2008_10
ORD IDord-df4888b4b1174495af4c2839637c72f6
Source noteuspto-grants-2008_10