関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Lithium Hydroxide | HCID 3939 | — |
| 反応物 | 1,1'-(Diazomethylene)bis(benzene) | HCID 61230 | — |
| 反応物 | Ethyl (R)-2-hydroxy-4-phenylbutyrate | HCID 2733848 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | benzhydryl (2R)-hydroxy-4-phenylbutyrate | HCID 54145254 | 38.4% |
反応手順
Dissolve (R)-2-hydroxy-4-phenylbutyric acid, ethyl ester (4.16 g, 20 mmol) in methanol (40 mL). Add 1N lithium hydroxide (25 mL, 25 mmol) and stir under an atmosphere of argon for 3.5 hours. Acidify with 1N hydrochloric acid (25 mL), saturate with sodium chloride and extract with ethyl acetate (3×25 mL). Combine the organic phases, dry (MgSO4) and evaporate the solvent in vacuo. Take up the residue in methylene chloride (20 mL) and add diphenyldiazomethane (3.36 g, 17.3 mmol). Stir overnight and wash with saturated sodium hydrogen carbonate (2×). Dry (MgSO4), evaporate the solvent in vacuo and recrystallize (methylene chloride/hexane then again with cyclohexane) to give (R)-2-hydroxy-4-phenylbutyric acid, diphenylmethyl ester as white needles (2.3 g, 38%); mp 82°-84° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05389628 |
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| 出典データセット | uspto-grants-1995_02 |
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| ORD ID | ord-377c9589bc794dde8794dfeef371643d |
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| 出典メモ | uspto-grants-1995_02 |
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