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

Thionyl Chloride → HCID 13772106、化合物

HRID 235573
ノート
印刷プレビュー

反応式

HRID 235573 の反応式
[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10]([O-:13])(=O)=[O:11])=[CH2:3].[K+].S(Cl)([Cl:17])=O>CN(C)C=O>[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10]([Cl:17])(=[O:13])=[O:11])=[CH2:3]
参加物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 24386Thionyl ChlorideHCID 23687389HCID 23687389、化合物

生成物 1

HCID 13772106HCID 13772106、化合物

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A mixture of potassium 2-(1-methylethenyl)benzenesulfonate (7.8 g, 0.33 mmol) and 30 ml of thionyl chloride was contacted with 1.5 ml of N,N-dimethylformamide at 0°. The mixture was allowed to warm to room temperature over 45 minutes then evaporated in vacuo. Water and ether were added and the aqueous phase extracted with several portions of ether. The combined ether layers were washed with saturated sodium chloride solution, dried and evaporated under reduced pressure to yield the title compound as an oil.

後処理

  1. customthen evaporated in vacuo
  2. additionWater and ether were added
  3. extractionthe aqueous phase extracted with several portions of ether
  4. washThe combined ether layers were washed with saturated sodium chloride solution
  5. customdried
  6. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-8a2d798c55cd491c8f55126071f8f399
出典データセット
uspto-grants-1987_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04640704

反応ノート

読み込み中…

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