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

Methane → 2-(3-Chlorophenylthio)benzoic acid

HRID 2226200
ノート
印刷プレビュー

反応式

HRID 2226200 の反応式
[C:1](=[O:4])([O-])[O-:2].[K+].[K+].Br[C:8]1[CH:9]=[C:10]([Cl:14])[CH:11]=[CH:12][CH:13]=1.O.[CH4:16].C[S:18]([CH3:20])=O>>[Cl:14][C:10]1[CH:9]=[C:8]([S:18][C:20]2[CH:12]=[CH:13][CH:8]=[CH:9][C:16]=2[C:1]([OH:2])=[O:4])[CH:13]=[CH:12][CH:11]=1
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 5

HCID 297MethaneHCID 679Dimethyl SulfoxideHCID 962WaterHCID 79281-Bromo-3-chlorobenzeneHCID 11430Potassium Carbonate

生成物 1

HCID 834292-(3-Chlorophenylthio)benzoic acid収率 86%

実験手順

A mixture of thiosolicyclic acid (50.14 g, 0.33 mol) and cupric acetate (5.0 g) in DMSO (500 mL) was brought to reflux and potassium carbonate (54.3 g) was added in portions. 3-Bromochlorobenzene (42 mL, 0.36 mol) was then added via syringe and the mixture was refluxed for 3 hours. The reaction mixture was poured into water, treated with charcoal and filtered through celite. The filtrate was acidified with concentrated HCl and the precipitate which formed was collected by filtration, washed with water and dried in vacuo at 60° C. to afford 75.01 g (86%) of 2-[(3-chlorophenyl)thio]benzoic acid.

後処理

  1. temperatureto reflux
  2. temperaturethe mixture was refluxed for 3 hours
  3. filtrationfiltered through celite
  4. customthe precipitate which formed
  5. filtrationwas collected by filtration
  6. washwashed with water
  7. customdried in vacuo at 60° C.

出典と根拠

ORDレコード
ord-faf36fb7d15c41e1bcbd014cd53ab32e
出典データセット
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05346917

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