Hydrogen Bromide → (R)-1-Methyl-1,2,3,4-tetrahydroisoquinoline
반응식
[CH3:1][C@@H:2]([NH2:9])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.Br[CH2:11][CH2:12]O.Br>ClCCl>[CH3:1][C@@H:2]1[C:3]2[C:8](=[CH:7][CH:6]=[CH:5][CH:4]=2)[CH2:12][CH2:11][NH:9]1참가 물질
반응 조건
- 온도
- 51 °C
실험 절차
76.61 g(630 mmole) of (R)-(+)-α-methylbenzylamine was dissolved in 77 ml of dichloromethane and 94.8 g(760 mmole) of 2-bromoethanol was added thereto. This mixture was stirred at 51° C. for 50 hours to complete the reaction. The reaction solution was concentrated under reduced pressure and 286.4 ml(2500 mmole) of 48% aqueous hydrobromic acid solution was added thereto and then allowed to react at 126° C. for 30 minutes under refluxing. The reaction solution was then distilled for 2 hours under normal pressure at constant temperature and 250 ml of aqueous hydrobromic acid and water, the reaction by-product, was removed. The residue was dissolved in 350 ml of isopropyl alcohol with refluxing for 30 minutes, and this solution was cooled to 10° C. and then allowed to stand for 3 hours. The resulting solid product was filtered, washed with 50 ml of ethyl acetate, and then dried to obtain 127.5 g of the title compound.
후처리
- customthe reaction
- additionwas added
- customto react at 126° C. for 30 minutes
- temperatureunder refluxing
- distillationThe reaction solution was then distilled for 2 hours under normal pressure at constant temperature and 250 ml of aqueous hydrobromic acid and water
- customthe reaction by-product, was removed
- dissolutionThe residue was dissolved in 350 ml of isopropyl alcohol
- temperaturewith refluxing for 30 minutes
- temperaturethis solution was cooled to 10° C.
- waitto stand for 3 hours
- filtrationThe resulting solid product was filtered
- washwashed with 50 ml of ethyl acetate
- customdried
출처 및 근거
- ORD 기록
- ord-6752f4f07c894881bd3b12a98a6ce577
- 출처 데이터셋
- uspto-grants-1999_11
- 특허 번호
- US05990311
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