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HRID 261747作成日:2026年10月27日

Benzyl Alcohol → Benzyl (2S)-hydroxy(phenyl)acetate

https://huagongshe.com/reaction/261747

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl AlcoholHCID 244—
反応物p-Toluenesulfonic acidHCID 6101—
反応物(S)-mandelic acidHCID 439616—
溶媒BenzeneHCID 241—
生成物Benzyl (2S)-hydroxy(phenyl)acetateHCID 66742342%

反応条件

温度10 °C

反応手順

L-Mandelic acid (10 g.), 6.91 g. of benzyl alcohol, and 75 mg. of p-toluenesulfonic acid in 70 ml. of benzene was refluxed under a Dean-Stark trap for a total of 28 hours on 4 consecutive days. The crude benzyl ester was obtained by successively concentrating the liquor and cooling it to about 10° C. a number of times. The fractions melting between 97° C. and 105° C. were combined, dissolved in CHCl3 and washed twice with 15-ml. portions of 5% aqueous NaHCO3 solution. After evaporation of the CHCl3, the product was recrystallized from benzene to give benzyl L-mandelate, m.p. 104°-106° C., yield 42%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04152333
出典データセットuspto-grants-1979_05
ORD IDord-a6485282a9a34f2983b7b57db745df81
出典メモuspto-grants-1979_05