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Sodium hydride → 2-Chloromethyl-2-(2-fluoro-4-trifluoromethylphenyl)oxirane

HRID 1732151
ノート
印刷プレビュー

反応式

HRID 1732151 の反応式
[Cl:1][CH2:2][C:3]([C:7]1[CH:12]=[CH:11][C:10]([C:13]([F:16])([F:15])[F:14])=[CH:9][C:8]=1[F:17])([OH:6])[CH2:4]Cl.[H-].[Na+]>C(O)(C)(C)C>[Cl:1][CH2:2][C:3]1([C:7]2[CH:12]=[CH:11][C:10]([C:13]([F:16])([F:15])[F:14])=[CH:9][C:8]=2[F:17])[CH2:4][O:6]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24758Sodium hydrideHCID 202266801,3-Dichloro-2-(2-fluoro-4-trifluoromethylphenyl)-2-propanol

生成物 1

HCID 202267062-Chloromethyl-2-(2-fluoro-4-trifluoromethylphenyl)oxirane

試薬・触媒・溶媒 1

HCID 6386tert-Butanol溶媒

反応条件

温度
100 °C

実験手順

1,3-Dichloro-2-(2-fluoro-4-trifluoromethylphenyl)-2-propanol (7 g.) was added to a solution of sodium hydride (1.45 g. of 48% dispersion in oil) in tert-butyl alcohol (30 ml.) and heated at 100° C. for 1 hour. The mixture was evaporated to dryness and the residue was partitioned between ethyl acetate and water. The organic layer was separated, washed with water and dried with anhydrous magnesium sulphate, and the filtered solution was evaporated to dryness to give 2-chloromethyl-2-(2-fluoro-4-trifluoromethylphenyl)oxirane as a yellow oil.

後処理

  1. customThe mixture was evaporated to dryness
  2. customthe residue was partitioned between ethyl acetate and water
  3. customThe organic layer was separated
  4. washwashed with water
  5. dry with materialdried with anhydrous magnesium sulphate
  6. customthe filtered solution was evaporated to dryness

出典と根拠

ORDレコード
ord-14125b150e614f768159db7134bf899e
出典データセット
uspto-grants-1986_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04625036

反応ノート

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