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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 512808Erstellt: 24. Oktober 2026

Benzyl Chloride → Methyl 2-(benzyloxy)propanoate

https://huagongshe.com/de/reaction/512808

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl ChlorideHCID 7503—
EduktMethyl LactateHCID 11040—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 2-(benzyloxy)propanoateHCID 561764—

Reaktionsschritte

To a pre-cooled solution of potassium tertiary butoxide (538.4 g) in DMF (1750 ml) at −20 to −10° C., added racemic methyl lactate compound of formula-11 (500 g) followed by benzyl chloride (547 g) at −20 to −10° C. and the reaction mixture was stirred for 5 hours at the same temperature. After completion of the reaction, the reaction mixture was quenched with water and the reaction mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water and 10% sodium chloride solution and then distilled off the solvent from ethyl acetate layer under reduced pressure to get the title compound as a residue. The obtained residue was taken into next step without isolation.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09102664B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-36e5364bb8604b519f3405652f340859
Quellennotizuspto-grants-2015_08