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HRID 512808作成日:2026年10月26日

Benzyl Chloride → Methyl 2-(benzyloxy)propanoate

https://huagongshe.com/reaction/512808

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl ChlorideHCID 7503—
反応物Methyl LactateHCID 11040—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DimethylformamideHCID 6228—
生成物Methyl 2-(benzyloxy)propanoateHCID 561764—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09102664B2
出典データセットuspto-grants-2015_08
ORD IDord-36e5364bb8604b519f3405652f340859
出典メモuspto-grants-2015_08