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Ammonium Chloride → (6-Fluoro-3-iodo-2-methylphenyl)methanol

HRID 1948670
ノート
印刷プレビュー

反応式

HRID 1948670 の反応式
[F:1][C:2]1[C:7]([C:8](OC)=[O:9])=[C:6]([CH3:12])[C:5]([I:13])=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl-].[NH4+].[H][H]>C(OCC)C>[F:1][C:2]1[C:7]([CH2:8][OH:9])=[C:6]([CH3:12])[C:5]([I:13])=[CH:4][CH:3]=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 25517Ammonium Chloride2 回HCID 21226445Aluminium lithium hydrideHCID 59450535Methyl 6-fluoro-3-iodo-2-methylbenzoateHCID 178418361HCID 178418361、化合物

生成物 1

HCID 59450541(6-Fluoro-3-iodo-2-methylphenyl)methanol

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒
このページの内容参加物実験手順後処理出典と根拠反応ノート

実験手順

To a solution of the product from Step B (5.5 g, 18.7 mmol) in diethyl ether (20 ml) was carefully added lithium aluminum hydride (0.8 g, 18.7 mmol). The mixture was stirred at room temperature for 16 h. Saturated aqueous ammonium chloride solution was added dropwise until no hydrogen gas was being generated. A few more drops of saturated aqueous ammonium chloride solution were added and the mixture was stirred at room temperature for 30 min and filtered. The filtrated was dried over magnesium sulfate and concentrated to dryness to give the title compound as a colorless oil.

後処理

  1. stirringthe mixture was stirred at room temperature for 30 min
  2. filtrationfiltered
  3. dry with materialThe filtrated was dried over magnesium sulfate
  4. concentrationconcentrated to dryness

出典と根拠

ORDレコード
ord-1fd73c74585946c8ba71ff1a9c74a445
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08399507B2

反応ノート

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