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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593335Generated: October 26, 2026

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

https://huagongshe.com/reaction/593335

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. 4.18 g (88%) of (RS)-5-(3-bromo-phenyl)-5-methyl-morpholin-3-one were obtained as a white solid. Mass (calculated) C11H12BrNO2 [270.128]; (found) [M+H]+=270 and [M+2+H]+=272.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242943B2
Source datasetuspto-grants-2016_01
ORD IDord-a21957b6e82846cea0a987a0688435e0
Source noteuspto-grants-2016_01