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Water → (4-Fluorophenyl)(2-thienyl)methanol

HRID 439831
ノート
印刷プレビュー

反応式

HRID 439831 の反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].[F:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]([C:16]2[S:17][CH:18]=[CH:19][CH:20]=2)=[O:15])=[CH:10][CH:9]=1.O.[OH-].[Na+]>C1COCC1>[F:7][C:8]1[CH:13]=[CH:12][C:11]([CH:14]([C:16]2[S:17][CH:18]=[CH:19][CH:20]=2)[OH:15])=[CH:10][CH:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962Water2 回HCID 14798Sodium HydroxideHCID 684794-Fluorophenyl 2-thienyl ketoneHCID 21226445Aluminium lithium hydride

生成物 1

HCID 10987480(4-Fluorophenyl)(2-thienyl)methanol収率 99%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran
溶媒

実験手順

Lithium aluminium hydride (3.68 g, 97 mmol) was added portionwise to a stirred solution of (4-fluorophenyl)-(2-thienyl)ketone (10.0 g, 48.5 mmol) in dry THF (160 ml) at room temperature under argon. The mixture was stirred overnight and water (3.7 ml) added dropwise with caution. After 0.5 h 15% aqueous sodium hydroxide (3.7 ml) was added and the mixture stirred for 0.5 h, finally water (11 ml) was added and the mixture stirred for 0.5 h. The precipitate was removed by filtration through celite and the flitrate was concentrated under reduced pressure to give (4-fluorophenyl)-(2-thienyl)methanol (10.0 g, 99%) as a yellow oil.

後処理

  1. stirringthe mixture stirred for 0.5 h
  2. stirringthe mixture stirred for 0.5 h
  3. customThe precipitate was removed by filtration through celite
  4. concentrationthe flitrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-f1789b4911b546f191c323347b3f4f65
出典データセット
uspto-grants-1996_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05516783

反応ノート

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