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HRID 247838作成日:2026年10月27日

Hydrochloric Acid → benzhydryl (2R)-hydroxy-4-phenylbutyrate

https://huagongshe.com/reaction/247838

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Lithium HydroxideHCID 3939—
反応物1,1'-(Diazomethylene)bis(benzene)HCID 61230—
反応物Ethyl (R)-2-hydroxy-4-phenylbutyrateHCID 2733848—
溶媒MethanolHCID 887—
生成物benzhydryl (2R)-hydroxy-4-phenylbutyrateHCID 5414525438.4%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05208230
出典データセットuspto-grants-1993_05
ORD IDord-6c28df1164f149b7803df0b1cbc39af2
出典メモuspto-grants-1993_05