Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methyl 1,2,3,4-tetrahydro-3-quinolinecarboxylate → (1,2,3,4-Tetrahydroquinolin-3-yl)methanol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methyl 1,2,3,4-tetrahydro-3-quinolinecarboxylate | HCID 283526 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | (1,2,3,4-Tetrahydroquinolin-3-yl)methanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07608618B2 |
| 출처 데이터셋 | uspto-grants-2009_10 |
| ORD ID | ord-859ea2becbb34bfb923c5ae704696c1d |
| 출처 메모 | uspto-grants-2009_10 |