Water → 4,6-Di-tert-butyl-2,2-diethyl-5-hydroxy-2,3-dihydrobenzofuran

HRID 1452363노트

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HRID 1452363 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].C([O:10][C:11]1[C:12]([C:28]([CH3:31])([CH3:30])[CH3:29])=[CH:13][C:14]2[O:18][C:17]([CH2:21][CH3:22])([CH2:19][CH3:20])[CH2:16][C:15]=2[C:23]=1[C:24]([CH3:27])([CH3:26])[CH3:25])(=O)C.O.[OH-].[Na+]>O1CCCC1>[C:24]([C:23]1[C:15]2[CH2:16][C:17]([CH2:19][CH3:20])([CH2:21][CH3:22])[O:18][C:14]=2[CH:13]=[C:12]([C:28]([CH3:29])([CH3:31])[CH3:30])[C:11]=1[OH:10])([CH3:25])([CH3:27])[CH3:26]

참가 물질

6

실험 절차

Lithium aluminum hydride (76 mg) was suspended in tetrahydrofuran (5 ml) under a nitrogen atmosphere. A solution of 5-acetoxy-4,6-di-tert-butyl-2,2-diethyl-2,3-dihydrobenzofuran (0.17 g, 0.5 mmol) in tetrahydrofuran (5 ml) was added dropwise to the suspension. After heating under reflux for 3 h, the reaction mixture was cooled to room temperature and water was added dropwise. After addition of 1N aqueous sodium hydroxide (5 ml), the mixture was subjected to extraction with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The concentrate was purified by silica gel chromatography (10% ethyl acetate in n-hexane) to afford 4,6-di-tert-butyl-2,2-diethyl-5-hydroxy-2,3-dihydrobenzofuran [130 mg (yield, 87%)] as a pale yellow oil.

후처리

  1. temperatureAfter heating
  2. temperatureunder reflux for 3 h
  3. extractionthe mixture was subjected to extraction with diethyl ether
  4. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  5. concentrationconcentrated
  6. customThe concentrate was purified by silica gel chromatography (10% ethyl acetate in n-hexane)

출처 및 근거

ORD 기록
ord-9a59f57a4fca448b8eb8786fa519473a
출처 데이터셋
uspto-grants-1997_02
특허 번호
US05606089

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