반응 #48904

반응 방정식

Hydrochloric acid

1-[3-(Cyclopentyloxy)-2-hydroxy-4-methoxyphenyl]ethanone

sodium hydride

diethyl carbonate

potassium t-butoxide

Potassium t-butoxide

→

8-(cyclopentyloxy)-4-hydroxy-7-methoxy-2H-chromen-2-one

용매

water

반응 조건

후처리

1. 1
   온도The reaction was refluxed for 1 h
2. 2
   추출extracted with ethyl acetate (200 mL×2)
3. 3
   기타The combined extracts were dried
4. 4
   여과filtered
5. 5
   농축concentrated
6. 6
   workup.DISSOLUTIONredissolved in t-butanol (50 mL)
7. 7
   온도the reaction was refluxed
8. 8
   workup.WAITAfter 42 h
9. 9
   workup.WAITAfter an additional 2 d
10. 10
    온도to cool to rt
11. 11
    농축concentrated
12. 12
    workup.ADDITIONdiluted with 1N HCl (100 mL)
13. 13
    추출extracted with ethyl acetate (200 mL×2)
14. 14
    기타The combined extracts were dried
15. 15
    여과filtered
16. 16
    농축concentrated
17. 17
    기타purified by silica gel chromatography (3:2→0:1; hexanes:ethyl acetate)

실험 절차

1-[3-(Cyclopentyloxy)-2-hydroxy-4-methoxyphenyl]ethanone (4.25 g, 17 mmol) was added portionwise to a mixture of sodium hydride (1.4 g, 60%, 35 mmol) and diethyl carbonate (30 mL) at rt under N2. The reaction was refluxed for 1 h and then cooled to rt. 10% Hydrochloric acid (30 mL) was added, and the mixture was stirred for 1 h. The reaction was diluted with water (100 mL) and extracted with ethyl acetate (200 mL×2). The combined extracts were dried, filtered, concentrated, and redissolved in t-butanol (50 mL). Potassium t-butoxide (4.0 g, 36 mmol) was added, and the reaction was refluxed. After 42 h, additional potassium t-butoxide (2.0 g, 18 mmol) was added. After an additional 2 d, the reaction was allowed to cool to rt, concentrated, diluted with 1N HCl (100 mL), and extracted with ethyl acetate (200 mL×2). The combined extracts were dried, filtered, concentrated, and purified by silica gel chromatography (3:2→0:1; hexanes:ethyl acetate) to give 8-(cyclopentyloxy)-4-hydroxy-7-methoxy-2H-chromen-2-one: MS (ESI): 277.1.

출처