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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946903Generated: November 1, 2026

Methanol → 5-(3-Bromophenyl)-5-methylmorpholin-3-one

https://huagongshe.com/reaction/1946903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantN-[1-(3-Bromophenyl)-2-hydroxy-1-methylethyl]-2-chloroacetamideHCID 58155284—
Solvent2-Methyl-2-butanolHCID 6405—
Product5-(3-Bromophenyl)-5-methylmorpholin-3-oneHCID 5815530591%

Reaction Steps

A solution of (RS)—N-[1-(3-bromo-phenyl)-2-hydroxy-1-methyl-ethyl]-2-chloro-acetamide (5.36 g, 17 mmol) in 2-methyl-2-butanol (100 ml) was treated in one portion with potassium tert-butylate (6.66 g, 58 mmol). Initially, the temperature rose to 30° C.; the reaction mixture was left to cool to room temperature and stirring was continued for one hour. For the workup, the reaction mixture was treated with methanol (50 ml), then evaporated at reduced pressure. The residue was purified by chromatography on silica gel using a gradient of dichloromethane/methanol=100/0 to 75/25 as the eluent. There were obtained 4.18 g (88% of theory) of (RS)-5-(3-bromo-phenyl)-5-methyl-morpholin-3-one as a white solid. MS (ISP): m/z=270.1 [M+H]+, 272.2 [M+2+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399459B2
Source datasetuspto-grants-2013_03
ORD IDord-32efdedf02074fe1b9719abf51933ff6
Source noteuspto-grants-2013_03