돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127578생성일: 2026년 10월 26일

Thionyl Chloride → HCID 56629765, 화합물

https://huagongshe.com/reaction/127578

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물3-(Benzoylthio)-2-methylpropanoic acidHCID 569497—
반응물methyl (3S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochlorideHCID 2760578—
반응물(1)-S-(3-Chloro-2-methyl-3-oxopropyl) benzenecarbothioateHCID 12878433—
용매ChloroformHCID 6212—
용매TriethylamineHCID 8471—
생성물HCID 56629765HCID 5662976580.5%

반응 단계

5.69 g of methyl (3S)-1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride are suspended in 50 ml of chloroform, and 5.6 g of triethylamine are added thereto under ice-cooling and stirring. 3-benzoylthio-2-methylpropionyl chloride (which is prepared by heating a mixture of 5.6 g of 3-benzoylthio-2-methyl-propionic acid and 6 ml of thionyl chloride at 60° C. for 2 hours, followed by distillation thereof to remove the excess of thionyl chloride) is dissolved in 10 ml of tetrahydrofuran, and said tetrahydrofuran solution is added dropwise to the suspension obtained above. After the mixture is stirred at room temperature overnight, the chloroform layer is collected therefrom and washed with water, an aqueous sodium bicarbonate solution, diluted hydrochloric acid and water, successively. The chloroform solution is dried and then distilled to remove solvent. The residue thus obtained is purified by silica gel column chromatography (Solvent, toluene-ethyl acetate (4:1)). 8.0 g of methyl (3S)-2-(3-benzoylthio-2-methylpropionyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylate are obtained as colorless oil. Yield: 80.5 %

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04256751
출처 데이터셋uspto-grants-1981_03
ORD IDord-2813aaff273042e3820a4bb2b0273ddf
출처 메모uspto-grants-1981_03