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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584228Generated: October 26, 2026

Chloroacetyl chloride → 4-Benzyl-5-(hydroxymethyl)-5-methylmorpholin-3-one

https://huagongshe.com/reaction/584228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Benzylamino)-2-methylpropane-1,3-diolHCID 198739—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-Benzyl-5-(hydroxymethyl)-5-methylmorpholin-3-oneHCID 22342739—

Reaction Steps

Chloroacetyl chloride (14.0 ml) was added dropwise to a mixture of 2-benzylamino-2-methyl-1,3-propanediol (28.5 g), potassium carbonate (30.3 g) in dichloromethane (150 ml) and water (150 ml) at 0° C., and the whole was stirred at room temperature for 2 hours. The mixture was extracted with dichloromethane and the extract was washed successively with water, 1N hydrochloric acid and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was dissolved in tert-butanol (400 ml) and the solution was added potassium tert-butoxide (16.38 g) portionwisely and the whole was refluxed for 30 minutes. After cooling, the solvent was removed by evaporation and ethyl acetate and water were added thereto. The organic layer was separated, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by column chromatography on silica gel with a mixture of ethyl acetate and n-hexane (1:1) as an eluent to give 4-benzyl-5-hydroxymethyl-5-methyl-3-morpholinone (10.89 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924278B2
Source datasetuspto-grants-2005_08
ORD IDord-75473a4fa51645e18d3a4f6e822d4c71
Source noteuspto-grants-2005_08