참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Lithium Hydroxide | HCID 3939 | — |
| 반응물 | 1,1'-(Diazomethylene)bis(benzene) | HCID 61230 | — |
| 반응물 | Ethyl (R)-2-hydroxy-4-phenylbutyrate | HCID 2733848 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | benzhydryl (2R)-hydroxy-4-phenylbutyrate | HCID 54145254 | 38.4% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05389628 |
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| 출처 데이터셋 | uspto-grants-1995_02 |
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| ORD ID | ord-377c9589bc794dde8794dfeef371643d |
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| 출처 메모 | uspto-grants-1995_02 |
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