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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276112생성일: 2026년 10월 27일

Hydrochloric Acid → 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine

https://huagongshe.com/reaction/276112

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물MethanolHCID 887—
반응물Lithium HydroxideHCID 3939—
반응물2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl esterHCID 22950828—
용매TetrahydrofuranHCID 8028—
용매Ethyl acetate hexaneHCID 21226206—
생성물2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanineHCID 22950827—

반응 단계

Combine 2-(4-methoxybenzylthio)-pentanoyl-(L)-homophenylalanine methyl ester (3.50 g, 8.15 mmol) and methanol (30 mL)and tetrahydrofuran (30 (mL). Cool in an ice bath. Add an aqueous 2M lithium hydroxide solution (8.2 mL, 16.4 mmol). After 18 hours, adjust the pH to about 6 using an aqueous 10% hydrochloric acid solution and evaporate in vacuo to give a residue. Partition the residue between dichloromethane and water, adjust the pH of the aqueous layer to about 1 using an aqueous 10% hydrochloric acid solution. Separate the layers, extract the aqueous layer repeatedly with ethyl acetate. Combine the organic layers, dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 95% 1/1 hexane/ethyl acetate/5% acetic acid to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06352976B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-222d2ac6f50248dabfb0e58127fe60d6
출처 메모uspto-grants-2002_03