Реакция #50422

Уравнение реакции

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

Растворители

water

water

Условия реакции

Обработка

1. 1
   workup.DISSOLUTIONto dissolve the solid
2. 2
   workup.STIRRINGwas stirred at room temperature for 20 hours after which it
3. 3
   ЭкстракцияThe mixture was then extracted with methylene chloride
4. 4
   СушкаThe extract was dried over sodium sulfate
5. 5
   Другоеevaporated
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
   ТемператураThe mixture then was refluxed for 1.5 hours after which it
9. 9
   workup.ADDITIONwas poured into water
10. 10
    Экстракцияextracted with methylene chloride
11. 11
    ЭкстракцияThe methylene chloride extract
12. 12
    Сушкаwas dried over sodium sulfate
13. 13
    Другоеevaporated

Методика

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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