関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzyl Alcohol | HCID 244 | — |
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | (S)-mandelic acid | HCID 439616 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | Benzyl (2S)-hydroxy(phenyl)acetate | HCID 667423 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04152333 |
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| 出典データセット | uspto-grants-1979_05 |
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| ORD ID | ord-a6485282a9a34f2983b7b57db745df81 |
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| 出典メモ | uspto-grants-1979_05 |
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