Реакция #1005935

Уравнение реакции

ethyl acetate

lithium-aluminum hydride

2-butin-1-ol

tri(n-butyl)stannyl-methanolate

→

(Z)-3-Tributylstannanyl-but-2-en-1-ol

Растворители

water

THF

THF

methanol

Условия реакции

Обработка

1. 1
   Другоеhas been lowered to 0° C.
2. 2
   workup.STIRRINGStirring
3. 3
   workup.STIRRINGwhile stirring
4. 4
   ДругоеA strongly exothermic reaction
5. 5
   workup.STIRRINGStirring
6. 6
   workup.WAITwas continued for 10 min
7. 7
   Температураwithout cooling
8. 8
   workup.STIRRINGwhile stirring
9. 9
   workup.STIRRINGStirring
10. 10
    workup.WAITwas continued for 2 d at 4° C
11. 11
    workup.WAITwas continued for 1 h at ambient temperature
12. 12
    Экстракцияextracted thrice with 150 ml diethyl ether each, the combined extracts
13. 13
    Промывкаwere washed twice with 80 ml of water each, then once with 40 ml saturated aqueous sodium chloride solution
14. 14
    Сушкаdried with sodium sulfate
15. 15
    Концентрированиеconcentrated in vacuo
16. 16
    ДругоеYield 48.6 g oil, which have been purified by chromatography on 300 g silica gel with hexane/MTBE (10:1)

Методика

To 156.9 ml (156.9 mmol) of a 1 molar solution of lithium-aluminum-hydride in THF 0.77 g (14.3 mmol) sodium methylate have been added and the temperature has been lowered to 0° C. afterwards. Then a solution of 10.0 g (142.7 mmol) 2-butin-1-ol in 108 ml THF has been added dropwise with stirring at this temperature. Stirring was continued for 36 h at 4° C. Thereafter, at about 0° C., 28.6 ml (292.5 mmol) ethyl acetate was-added slowly while stirring. A strongly exothermic reaction was observed. Stirring was continued for 10 min without cooling. After cooling to about 0° C., 45.8 g (142.7 mmol) tri(n-butyl)stannyl-methanolate have been added dropwise while stirring. Stirring was continued for 2 d at 4° C. After addition of 112.9 g methanol stirring was continued for 1 h at ambient temperature. The reaction mixture was poured into 250 ml of water, extracted thrice with 150 ml diethyl ether each, the combined extracts were washed twice with 80 ml of water each, then once with 40 ml saturated aqueous sodium chloride solution, dried with sodium sulfate and concentrated in vacuo. Yield 48.6 g oil, which have been purified by chromatography on 300 g silica gel with hexane/MTBE (10:1). Final yield 34.6 g (67%) oil. δ=0.90 (m); 1.30 (m); 1.50 m); 1.97 (s); 4.02 (t); 6.27 (t).

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