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Methane → 2-(3-Chlorophenylthio)benzoic acid

HRID 2226200
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반응식

HRID 2226200 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 5

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

생성물 1

HCID 834292-(3-Chlorophenylthio)benzoic acid수율 86%

실험 절차

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.

후처리

  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.

출처 및 근거

ORD 기록
ord-faf36fb7d15c41e1bcbd014cd53ab32e
출처 데이터셋
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05346917

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