反应 #50422

反应方程式

Potassium t-butoxide

Ethyl formate

2-di-n-propylamino-8-butyryl-1,2,3,4-tetrahydronaphthalene

THF

ammonium hydroxide

Hydroxylamine

tetrahydrofuran

→

2-Di-n-propylamino-8-(4-ethylisoxazol-5-yl)-1,2,3,4-tetrahydronaphthalene

溶剂

water

water

反应条件

后处理

1. 1
   workup.DISSOLUTIONto dissolve the solid
2. 2
   workup.STIRRINGwas stirred at room temperature for 20 hours after which it
3. 3
   萃取The mixture was then extracted with methylene chloride
4. 4
   干燥The extract was dried over sodium sulfate
5. 5
   其他evaporated
6. 6
   workup.DISSOLUTIONThe residue was dissolved in 100 of toluene, and 100 mg of p-toluenesulfonic acid
7. 7
   workup.ADDITIONwas added
8. 8
   温度The mixture then was refluxed for 1.5 hours after which it
9. 9
   workup.ADDITIONwas poured into water
10. 10
    萃取extracted with methylene chloride
11. 11
    萃取The methylene chloride extract
12. 12
    干燥was dried over sodium sulfate
13. 13
    其他evaporated

实验过程

Potassium t-butoxide (0.82 g; 7.3 mmol) was suspended in 100 ml of tetrahydrofuran (THF). Ethyl formate (1.0 g; 13.3 mmol) and 2-di-n-propylamino-8-butyryl-1,2,3,4-tetrahydronaphthalene (1.0 g; 3.3 mmol) in THF was added to the mixture. The resulting mixture was stirred at room temperature overnight. Hydroxylamine (1.2 g; 16.6 mmol) was added followed by sufficient water to dissolve the solid. The resulting mixture, having pH 6, was stirred at room temperature for 20 hours after which it was poured into water, and the pH was adjusted to 12 with ammonium hydroxide. The mixture was then extracted with methylene chloride. The extract was dried over sodium sulfate and evaporated. The residue was dissolved in 100 of toluene, and 100 mg of p-toluenesulfonic acid was added. The mixture then was refluxed for 1.5 hours after which it was poured into water and extracted with methylene chloride. The methylene chloride extract was dried over sodium sulfate and evaporated.

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