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Potassium Sodium Tartrate → 3-chloro-N-ethyl-4-fluoroaniline

HRID 1974616
ノート
印刷プレビュー

反応式

HRID 1974616 の反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].[Cl:7][C:8]1[CH:9]=[C:10]([CH:15]=[CH:16][C:17]=1[F:18])[NH:11][C:12](=O)[CH3:13].[C@H](O)(C([O-])=O)[C@@H](O)C([O-])=O.[Na+].[K+]>CCOCC.C1COCC1>[Cl:7][C:8]1[CH:9]=[C:10]([CH:15]=[CH:16][C:17]=1[F:18])[NH:11][CH2:12][CH3:13]
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 3

HCID 9357Potassium Sodium TartrateHCID 589188N-(3-Chloro-4-fluorophenyl)acetamideHCID 21226445Aluminium lithium hydride

生成物 1

HCID 142024823-chloro-N-ethyl-4-fluoroaniline収率 97.5%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 8028
Tetrahydrofuran
溶媒

実験手順

A suspension of lithium aluminium hydride (44.1 g, 1.16 mmol) in absolute ether (700 ml) is treated dropwise with a solution of 3'-chloro-4'-fluoroacetanilide (BE Patent No. 891537; 109 g, 0.576 mol) in absolute THF (350 ml). The suspension obtained is stirred for 2 hours, then cooled to 0° and treated with a Rochelle salt solution (350 ml). The crystals obtained are filtered off and washed with ether. The organic solution is dried over magnesium sulphate and the solvent is distilled off under reduced pressure. There are obtained 97.5 g (97.5%) of 3-chloro-N-ethyl-4-fluoroaniline as an amorphous material.

後処理

  1. customThe suspension obtained
  2. temperaturecooled to 0°
  3. customThe crystals obtained
  4. filtrationare filtered off
  5. washwashed with ether
  6. dry with materialThe organic solution is dried over magnesium sulphate
  7. distillationthe solvent is distilled off under reduced pressure

出典と根拠

ORDレコード
ord-d75e15cedc8e4c92835accc47f92c250
出典データセット
uspto-grants-1994_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05283248

反応ノート

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