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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1032983생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1032983

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Lithium HydroxideHCID 3939—
반응물1,1'-(Diazomethylene)bis(benzene)HCID 61230—
반응물Ethyl (R)-2-hydroxy-4-phenylbutyrateHCID 2733848—
용매MethanolHCID 887—
생성물benzhydryl (2R)-hydroxy-4-phenylbutyrateHCID 5414525438.4%

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 (3×25mL). 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 (2X). 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05308841
출처 데이터셋uspto-grants-1994_05
ORD IDord-6ee2a9f2f73749b68e9f44a751fe5e7a
출처 메모uspto-grants-1994_05