반응 #6641

반응 방정식

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

용매

tetrahydrofuran

tetrahydrofuran

hexane

반응 조건

후처리

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

실험 절차

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).

출처