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Water → 2-Chloro-4-(n-pentyl)benzyl alcohol

HRID 1699906
ノート
印刷プレビュー

反応式

HRID 1699906 の反応式
[F-].C([N+](CCCC)(CCCC)CCCC)CCC.O1CCCC1.[Si]([O:41][CH2:42][C:43]1[CH:48]=[CH:47][C:46]([CH2:49][CH2:50][CH2:51][CH2:52][CH3:53])=[CH:45][C:44]=1[Cl:54])(C(C)(C)C)(C1C=CC=CC=1)C1C=CC=CC=1.O>O1CCCC1>[Cl:54][C:44]1[CH:45]=[C:46]([CH2:49][CH2:50][CH2:51][CH2:52][CH3:53])[CH:47]=[CH:48][C:43]=1[CH2:42][OH:41]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 11078149TBAF tetrahydrofuranHCID 223883821-((tert-Butyldiphenylsilyloxy)methyl)-2-chloro-4-(n-pentyl)benzene

生成物 1

HCID 536994732-Chloro-4-(n-pentyl)benzyl alcohol収率 82.2%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A solution (1.0 M, 2.4 ml) of tetrabutylammonium fluoride/tetrahydrofuran was added to a solution of 1-((tert-butyldiphenylsilyloxy)methyl)-2-chloro-4-(n-pentyl)benzene (890 mg) in tetrahydrofuran (4.5 ml) under ice-cooling, and the mixture was stirred for 2 hr. Water was added to the reaction mixture and the resulting product was extracted three times with ethyl acetate. The organic layers were combined and washed successively with diluted hydrochloric acid, a saturated aqueous solution of sodium hydrogencarbonate and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=7/1) to give the objective compound (345 mg) as a colorless oil.

後処理

  1. temperaturecooling
  2. extractionthe resulting product was extracted three times with ethyl acetate
  3. washwashed successively with diluted hydrochloric acid
  4. dry with materiala saturated aqueous solution of sodium hydrogencarbonate and saturated brine, and dried over anhydrous magnesium sulfate
  5. customThe solvent was evaporated
  6. customthe residue was purified by silica gel column chromatography (hexane/ethyl acetate=7/1)

出典と根拠

ORDレコード
ord-2ac7ff7cd62e4860b209d2be08f656c6
出典データセット
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06348474B1

反応ノート

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