ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Water → 1-(2,6-Dichloropyridin-4-YL)ethanone

HRID 1586387
ノート
印刷プレビュー

反応式

HRID 1586387 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:16]=[C:17]([Cl:19])[N:18]=1)[C:5]([CH:7](C(OC)=O)C(OC)=O)=[O:6].O>CS(C)=O>[C:5]([C:4]1[CH:3]=[C:2]([Cl:1])[N:18]=[C:17]([Cl:19])[CH:16]=1)(=[O:6])[CH3:7]
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 962WaterHCID 22119448Dimethyl (2,6-dichloropyridine-4-carbonyl)propanedioate

生成物 1

HCID 221194461-(2,6-Dichloropyridin-4-YL)ethanone収率 61.4%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

反応条件

温度
140 °C

実験手順

1328 g (4.34 mol) of dimethyl 2,6-dichloro-isonicotinoyl-malonate are dissolved in a mixture of 3.45 l of dimethyl sulphoxide and 156.2 g (8.68 mol) of water. The reaction mixture is heated to 140° C. and stirred at this temperature for 30 minutes. After this, the reaction mixture is cooled to 10° C. and then added to 8.4 l of ice-water. The mixture is extracted twice with a total of 3.6 l of dichloromethane and the combined organic phases are washed once with 1.5 l of saturated, aqueous sodium hydrogen carbonate solution. After drying over sodium sulphate, the organic phase is concentrated under reduced pressure. The residue which remains is distilled under reduced pressure. In this manner 506.0 g (60% of theory) of 4-acetyl-2,6-dichloropyridine of boiling point 98° C. at 0.5 mbar are obtained. ##STR36##

後処理

  1. temperatureAfter this, the reaction mixture is cooled to 10° C.
  2. extractionThe mixture is extracted twice with a total of 3.6 l of dichloromethane
  3. washthe combined organic phases are washed once with 1.5 l of saturated, aqueous sodium hydrogen carbonate solution
  4. dry with materialAfter drying over sodium sulphate
  5. concentrationthe organic phase is concentrated under reduced pressure
  6. distillationThe residue which remains is distilled under reduced pressure

出典と根拠

ORDレコード
ord-f9169ea51b064bf8953f9b2c4ddc419f
出典データセット
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05945380

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート