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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1821764생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1821764

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 LiAIH4 (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) δ 6.97 (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 번호US07608618B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-859ea2becbb34bfb923c5ae704696c1d
출처 메모uspto-grants-2009_10