反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A three neck 3-liter round bottom flask equipped with a mechanical stirrer, water condenser, and a gas inlet tube was charged with 500 ml. of absolute ethanol and chilled in a dry ice-acetone bath. Dry hydrogen chloride gas was added at a rapid rate for 0.5 hours. Fifty grams of 5-methoxyindole-2-carboxylic acid ethyl ester (B. Heath-Brown and P. G. Philpott, J. Chem. Soc. 1965, 7185) followed by 100 g. of tin metal (30 mesh) were added to the solution with stirring. With the dry ice bath in place, but with no additional cooling the reaction mixture was stirred gently for 6 hours. The crystalline solid that separated was removed by filtration. The mother liquor was evaporated under reduced pressure to give an oil. The oil dissolved in 500 ml. of absolute ethanol, was placed in a 3-liter round bottom flask equipped with a stirrer and thermometer, and chilled to 10°. Gaseous ammonia was bubbled into the mixture until the pH was 9 (by wet pH paper) and the mixture was allowed to stand at 10° for one hour. The while precipitate was filtered and the filtrate was evaporated on a rotary evaporator to dryness. The initial white precipitate and the residue from the evaporation were combined and triturated repeatedly with warm ether. The combined ether triturates were washed with a sodium chloride solution (a water:saturated salt solution, 1:1) with vigorous shaking; whereupon most of the basic tin salts were suspended and separated in the aqueous phase. Both phases were filtered through Celite and separated. The ether solution was dried over magnesium sulfate and evaporated under reduced pressure on the rotary evaporator. The oily residue was dried in vacuo to give 22 g. of d,1-2,3-dihydro-5-methoxy-1H-indole-2-carboxylic acid ethyl ester.
WORKUP
后处理
- customA three neck 3-liter round bottom flask equipped with a mechanical stirrer, water condenser, and a gas inlet tube
- additionwas charged with 500 ml
- stirringwas stirred gently for 6 hours
- customThe crystalline solid that separated
- customwas removed by filtration
- customThe mother liquor was evaporated under reduced pressure
- customto give an oil
- dissolutionThe oil dissolved in 500 ml
- customequipped with a stirrer
- temperaturethermometer, and chilled to 10°
- customGaseous ammonia was bubbled into the mixture until the pH was 9 (by wet pH paper)
- filtrationThe while precipitate was filtered
- customthe filtrate was evaporated on a rotary evaporator to dryness
- customThe initial white precipitate and the residue from the evaporation
- customtriturated repeatedly with warm ether
- washThe combined ether triturates were washed with a sodium chloride solution (a water
- customseparated in the aqueous phase
- filtrationBoth phases were filtered through Celite
- customseparated
- dry with materialThe ether solution was dried over magnesium sulfate
- customevaporated under reduced pressure on the rotary evaporator
- customThe oily residue was dried in vacuo
- customto give 22 g