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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1830749생성일: 2026년 10월 25일

Methyl 1,2,3,4-tetrahydro-3-quinolinecarboxylate → (1,2,3,4-Tetrahydroquinolin-3-yl)methanol

https://huagongshe.com/reaction/1830749

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 1,2,3,4-tetrahydro-3-quinolinecarboxylateHCID 283526—
용매Diethyl EtherHCID 3283—
생성물(1,2,3,4-Tetrahydroquinolin-3-yl)methanolHCID 12662987—

반응 단계

To a stirred solution of the 1,2,3,4-Tetrahydro-quinoline-3-carboxylic acid methyl ester (93 mg, 0.49 mmol) in 1.5 mL of Et2O at 0° C. under nitrogen was added LiA1H4 (1M in Et2O) dropwise with vigorous gas evolution and a white precipitate formation. After 30 min., the reaction was carefully quenched with 15% NaOH (3 mL) and 3 mL of Et2O was added and the mixture stirred rapidly at RT for 15 min. The layers were separated and the aqueous layer extracted (1×10 mL) with Et2O. The organics were combined, dried (MgSO4), filtered and concentrated to the alcohol (64 mg, 80%). 1H-NMR (400 MHz, CDCl3) δ6.97 (m, 2H), 6.62 (dd, 1H), 6.47 (d, 1H), 3.66 (m, 1H), 3.58 (m, 1H), 3.40 (m, 1H), 3.08 (m, 1H), 2.82 (m, 1H), 2.53 (m, 1H), 2.18 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07067506B2
출처 데이터셋uspto-grants-2006_06
ORD IDord-de70020df0f5406ba6baf410bb83de1b
출처 메모uspto-grants-2006_06