Imidazole → 4-[4-(t-Butyldimethylsilyl)oxy-2,6,6-trimethylcyclohex-1-enyl]but-3-en-2-one

HRID 703620노트

반응식

HRID 703620 반응식
CN(C)C=O.N1C=CN=C1.[OH:11][CH:12]1[CH2:17][C:16]([CH3:19])([CH3:18])[C:15]([CH:20]=[CH:21][C:22](=[O:24])[CH3:23])=[C:14]([CH3:25])[CH2:13]1.[C:26]([Si:30]([CH3:33])([CH3:32])Cl)([CH3:29])([CH3:28])[CH3:27]>C(OCC)C>[Si:30]([O:11][CH:12]1[CH2:17][C:16]([CH3:18])([CH3:19])[C:15]([CH:20]=[CH:21][C:22](=[O:24])[CH3:23])=[C:14]([CH3:25])[CH2:13]1)([C:26]([CH3:29])([CH3:28])[CH3:27])([CH3:33])[CH3:32]

참가 물질

6

실험 절차

To 30 ml of an anhydrous dimethylformamide (hereinafter "DMF") solution containing 588 mg of imidazole and 1.2 g of 4-(4-hydroxy-2,6,6-trimethylcyclohex-1-enyl)but-3-en-2-one was added dropwise 15 ml of an anhydrous DMF solution containing 1.3 g of t-butyldimethylchlorosilane at room temperature in a nitrogen atmosphere. After the dropwise addition, the mixture was stirred under the same conditions for 15 hours. Diethyl ether was added to the reaction mixture, and the mixture was washed several times with water cooled with ice. The organic layer was dried over anhydrous magnesium sulfate, and the solvent, etc. were removed by distillation under reduced pressure. The residue was purified by silica gel column chromatography to obtain 1.5 g (yield: 78%) of 4-[4-(t-butyldimethylsilyl)oxy-2,6,6-trimethylcyclohex-1-enyl]-but-3-en-2-one.

후처리

  1. additionAfter the dropwise addition
  2. washthe mixture was washed several times with water
  3. temperaturecooled with ice
  4. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  5. customthe solvent, etc. were removed by distillation under reduced pressure
  6. customThe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-d61367c28e8e430e8cb76c4270bde4b0
출처 데이터셋
uspto-grants-1991_01
특허 번호
US04983723

반응 노트

불러오는 중…