Реакция #6641

Уравнение реакции

diethyl chlorophosphate

lithium diisopropyl amide

n-butyllithium

diisopropylamine

n-butyl lithium

4,4-dimethyl-6-acetylchroman

Compound 77

4,4-dimethyl-6-acetylchroman

→

title compound

4,4-Dimethyl-6-ethynylchroman

Растворители

tetrahydrofuran

tetrahydrofuran

hexane

Условия реакции

Обработка

1. 1
   Сушкаdry of tetrahydrofuran
2. 2
   workup.STIRRINGAfter stirring at 31 78 degrees C
3. 3
   workup.WAITfor 1 hour
4. 4
   ДругоеThe cooling bath was then removed
5. 5
   workup.STIRRINGthe reaction mixture stirred at room temperature for 2.75 hours
6. 6
   Другоеat 31 78 degrees C
7. 7
   ДругоеThe cooling bath was removed
8. 8
   workup.STIRRINGmixture stirred at room temperature for 18 hours
9. 9
   Другоеquenched with 50 ml water and 25 ml of 3N hydrogen chloride The mixture
10. 10
    Экстракцияwas extracted with 2×100 ml and 3×50 ml of pentane
11. 11
    Промывкаthe combined organic fractions washed with 3N hydrogen chloride, water, saturated NaHCO3 and saturated NaCl solutions
12. 12
    Сушкаdried (MgSO4)
13. 13
    ДругоеSolvent was then removed in vacuo
14. 14
    Другоеthe residue purified by flash chromatography (silica; 10% ethyl acetate in hexane)
15. 15
    workup.DISTILLATIONfollowed by kugelrohr distillation (70 degrees C.; 0.35mm)

Методика

To a solution of 2.47 g (24.41 mmol) of diisopropylamine in 40 ml dry tetrahydrofuran under argon at 31 78 degrees C was added dropwise 15.2 ml of 1.6M (24.32 mmol) n-butyl lithium in hexane. This mixture was stirred at 31 78 degrees C. for 1 hour and then treated dropwise with a solution of 4.98 g (24.38 mmol) of 4,4-dimethyl-6-acetylchroman (Compound 77) in 1 ml dry of tetrahydrofuran. After stirring at 31 78 degrees C. for 1 hour, the solution was treated with 4.2 g (24.36 mmol) of diethyl chlorophosphate. The cooling bath was then removed and the reaction mixture stirred at room temperature for 2.75 hours. This solution was then transferred using a double ended needle to a solution of lithium diisopropyl amide [prepared using 4.95 g (48.92 mmol) or diisopropylamine and 30.5 ml of 1.6M (48.8 mmol) n-butyllithium in hexane] in 80 ml dry tetrahydrofuran at 31 78 degrees C. The cooling bath was removed and mixture stirred at room temperature for 18 hours and then quenched with 50 ml water and 25 ml of 3N hydrogen chloride The mixture was extracted with 2×100 ml and 3×50 ml of pentane and the combined organic fractions washed with 3N hydrogen chloride, water, saturated NaHCO3 and saturated NaCl solutions and then dried (MgSO4). Solvent was then removed in vacuo and the residue purified by flash chromatography (silica; 10% ethyl acetate in hexane) followed by kugelrohr distillation (70 degrees C.; 0.35mm) to give the title compound as a colorless crystalline solid. PMR (CDCl3): δ 1.33 (6H), 1.81-1.86 (2H, m), 3.00 (1H, s), 4.19-4.24 (2H, m), 6.75 (1H, d, J~8.5 Hz}, 7.22 (1H, dd, J~8.5 Hz, 2.3 Hz), 7.44 (1H, d, J~2 3 Hz).

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