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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 236337생성일: 2026년 10월 23일

Methanol → methyl (3S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride

https://huagongshe.com/ko/reaction/236337

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Thionyl ChlorideHCID 24386—
반응물1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acidHCID 95489—
생성물methyl (3S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochlorideHCID 2760578—

반응 단계

In succession 5 g of tetrahydroisoquinoline 3-carboxylic acid and 30 ml of methanol are introduced into a three-necked flask. 6 g of thionyl chloride are added to this suspension by pouring carefully, taking care that the temperature does not exceed 0, +5°. The addition takes approximately 10 minutes. After the addition is completed, stirring is continued for 2 hours at room temperature, and then the mixture is heated to reflux for 11/2 hours. Once the mixture has dissolved completely, heating is discontinued and the mixture is then evaporated to dryness. The residue is taken up three times in methanol and then evaporated to dryness. Finally, 8 g of colourless crystals are obtained and purified by trituration with ether. The crystals are separated off by filtration, washed with ether and dried. 6.4 g of methyl tetrahydroisoquinoline-3-carboxylate hydrochloride are thus obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04644008
출처 데이터셋uspto-grants-1987_02
ORD IDord-f6519eaa5551445a8f560472842abe6d
출처 메모uspto-grants-1987_02