Imidazole → 6-(2-tert-butyidimethylsilyloxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran
반응식
[OH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8][C:9]1[CH:21]=[CH:20][C:12]2[O:13][C:14]([CH3:19])([CH3:18])[C:15]([CH3:17])=[CH:16][C:11]=2[CH:10]=1.N1C=CN=C1.[Si:27](Cl)([C:30]([CH3:33])([CH3:32])[CH3:31])([CH3:29])[CH3:28].O>CN(C)C=O>[Si:27]([O:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8][C:9]1[CH:21]=[CH:20][C:12]2[O:13][C:14]([CH3:18])([CH3:19])[C:15]([CH3:17])=[CH:16][C:11]=2[CH:10]=1)([C:30]([CH3:33])([CH3:32])[CH3:31])([CH3:29])[CH3:28]참가 물질
반응 조건
- 온도
- 40 °C
실험 절차
6-(2-hydroxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran (1.1 g) (see Preparation 10) was dissolved in dry dimethylformamide (2 ml) and imidazole (0.55 g) and tert-butyldimethylsilyl chloride (0.61 g) were added. The flask was fitted with a calcium chloride drying tube and the mixture stirred at 40° C. for 90 minutes. Water was added and the mixture was extracted with diethyl ether. The organic extract was washed with aqueous sodium hydrogen carbonate solution (×2), dried (anhydrous sodium sulphate), the solvent removed under reduced pressure and the crude product was chromatographed on silica using 4:1 hexane: dichloromethane as the eluent to yield 6-(2-tert-butyidimethylsilyloxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran (1.43 g) as an oil.
후처리
- customThe flask was fitted with a calcium chloride drying tube
- extractionthe mixture was extracted with diethyl ether
- extractionThe organic extract
- washwas washed with aqueous sodium hydrogen carbonate solution (×2)
- dry with materialdried (anhydrous sodium sulphate)
- customthe solvent removed under reduced pressure
- customthe crude product was chromatographed on silica using 4:1 hexane
출처 및 근거
- ORD 기록
- ord-c45637a7b0184063b4263a63cd15881b
- 출처 데이터셋
- uspto-grants-1999_06
- 특허 번호
- US05912244
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