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Sodium Hydroxide → 5-Chloro-2-(trifluoromethyl)pyridine

HRID 1627726
ノート
印刷プレビュー

反応式

HRID 1627726 の反応式
N([C:3]1[C:8]([Cl:9])=[CH:7][CH:6]=[C:5]([C:10]([F:13])([F:12])[F:11])[N:4]=1)N.[OH-].[Na+].Cl[O-].[Na+]>ClCCl>[Cl:9][C:8]1[CH:3]=[N:4][C:5]([C:10]([F:12])([F:11])[F:13])=[CH:6][CH:7]=1
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 14798Sodium HydroxideHCID 23665760Sodium Hypochlorite2 回HCID 690210312-Hydrazino-3-chloro-6-trifluoromethyl pyridine

生成物 1

HCID 135326585-Chloro-2-(trifluoromethyl)pyridine収率 110.9%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

The remaining 2-hydrazino-3-chloro-6-trifluoromethyl pyridine (63.36 g, 0.299 mol) was dissolved in dichloromethane (600 g) and charged to a 2 L, three-neck flask with a mechanical stirrer. Sodium hydroxide (300 g, 1N solution) was added, and sodium hypochlorite (NaCl) (448 g, 0.301 mol, 5% solution) was added in one portion. The solution was stirred for three hours after addition of the sodium hypochlorite, at which point sampling indicated the reaction was complete. The layers were separated, and the aqueous layer was extracted twice with dichloromethane (150 mL). The organic layers were combined, washed with water, dried with magnesium sulfate, filtered, and concentrated on the rotovap to give 60.2 g of 3-chloro-6-trifluoromethyl pyridine.

後処理

  1. additioncharged to a 2 L, three-neck flask with a mechanical stirrer
  2. aliquotat which point sampling
  3. customThe layers were separated
  4. extractionthe aqueous layer was extracted twice with dichloromethane (150 mL)
  5. washwashed with water
  6. dry with materialdried with magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated on the rotovap

出典と根拠

ORDレコード
ord-c14a721481a040588e8509290e584b5d
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08785650B2

反応ノート

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