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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1171846생성일: 2026년 10월 27일

Toluene → benzyl (S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylate

https://huagongshe.com/reaction/1171846

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Potassium CarbonateHCID 11430—
반응물(1S)-1,2,3,4-Tetrahydro-1-phenylisoquinolineHCID 1382087—
반응물Benzylchloride carbonateHCID 23113504—
용매WaterHCID 962—
생성물benzyl (S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylateHCID 67078747—

반응 조건

온도20 °C

반응 단계

A 25.0 g portion of (S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline and 24.5 g of benzyl chloride carbonate were added to a mixture of 125 ml of toluene, 19.8 g of potassium carbonate and 75 ml of water and stirred at 20° C. for 4 hours, and the organic layer was washed with 75 ml of water. The thus obtained organic layer was concentrated under a reduced pressure, purified by a silica gel column chromatography and then dried to obtain 38.0 g of (S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline-2-carboxylic acid benzyl ester (1H-NMR (DMSO-d6, tetramethylsilane internal standard): δ 2.73-2.83 (1H, m), 2.84-2.94 (1H, m), 3.31-3.41 (1H, m), 3.86-3.96 (1H, m), 5.12 (1H, d, J=12.8 Hz), 5.18 (1H, d, J=12.8 Hz), 6.28 (1H, s), 7.10-7.38 (14H, m), mass spectrum: m/z=344 [M+H]+ (FAB)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07829715B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-8b943db39ead498a9237cd6a7468cd2f
출처 메모uspto-grants-2010_11