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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 584228Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/584228

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroacetyl chlorideHCID 6577—
EduktPotassium CarbonateHCID 11430—
Edukt2-(Benzylamino)-2-methylpropane-1,3-diolHCID 198739—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Benzyl-5-(hydroxymethyl)-5-methylmorpholin-3-oneHCID 22342739—

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06924278B2
Quelldatensatzuspto-grants-2005_08
ORD IDord-75473a4fa51645e18d3a4f6e822d4c71
Quellennotizuspto-grants-2005_08