Реакция #2235

Уравнение реакции

Acetyl chloride

methanol

1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

→

title compound

Выход 46.6%

3-Methoxycarbonyl-1,2,3,4-tetrahydroisoquinoline

Выход 46.6%

Растворители

DMF

Условия реакции

Обработка

1. 1
   Температураto warm to room temperature
2. 2
   workup.STIRRINGstirred overnight
3. 3
   workup.STIRRINGstirring
4. 4
   workup.WAITwas then continued for a further 24 h
5. 5
   ДругоеThe solvent was removed in vacuo
6. 6
   workup.ADDITIONdichloromethane was added
7. 7
   Другоеthe solid thus formed
8. 8
   Фильтрацияwas filtered off
9. 9
   Другоеpartitioned between dichloromethane (50 ml) and saturated aqueous sodium hydrogen carbonate solution (50 ml)
10. 10
    СушкаThe organic phase was dried (magnesium sulphate)
11. 11
    Фильтрацияfiltered
12. 12
    Другоеthe filtrate evaporated in vacuo

Методика

Acetyl chloride (0.88 g) was added to methanol (100 ml) with stirring at 0° C. After 10 minutes, 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (J. Am. Chem. Soc., 1962, 48, 4487-4494) (2.0 g) was added; the reaction was allowed to warm to room temperature and stirred overnight. DMF (1 ml) was then added and stirring was then continued for a further 24 h. The solvent was removed in vacuo; dichloromethane was added and the solid thus formed was filtered off and partitioned between dichloromethane (50 ml) and saturated aqueous sodium hydrogen carbonate solution (50 ml). The organic phase was dried (magnesium sulphate), filtered, and the filtrate evaporated in vacuo to yield the title compound as a pale yellow oil (1.0 g).

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