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Methane → 2-(3-Chlorophenylthio)benzoic acid

HRID 1769174
ノート
印刷プレビュー

反応式

HRID 1769174 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-832b6285415a4842ab042b8814ba3b40
出典データセット
uspto-grants-1995_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05380749

反応ノート

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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