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Pyridine → 2-(Naphthalen-2-ylthio)benzoic acid

HRID 616353
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HRID 616353 반응식
I[C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[SH:11][C:12]1[CH:21]=[CH:20][C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:13]=1.C(=O)([O-])[O-].[K+].[K+].N1C=CC=CC=1>O>[CH:13]1[C:14]2[C:19](=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:20]=[CH:21][C:12]=1[S:11][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 1049PyridineHCID 69412-Iodobenzoic acidHCID 70582-NaphthalenethiolHCID 11430Potassium Carbonate

생성물 1

HCID 122280962-(Naphthalen-2-ylthio)benzoic acid

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A well stirred mixture of 37.2 g. (0.15 mole) of o-iodobenzoic acid, 34.0 g. (0.15 mole) of 2-mercaptonaphthalene, 20.6 g. (0.15 mole) of potassium carbonate and 300 ml. of pyridine is heated at 50° C. for 1 hour, then 5 g. of cuprous chloride is added and the stirred mixture is heated at reflux for 18 hours. The mixture is poured into 1.2 liters of water and filtered. The filtrate is acidified and the resulting mixture is extracted into methylene chloride. The extracts are dried, concentrated, and the solid residue is recrystallized to give 2-(2-naphthylthio)benzoic acid.

후처리

  1. additionmixture of 37.2 g
  2. temperaturethe stirred mixture is heated
  3. temperatureat reflux for 18 hours
  4. filtrationfiltered
  5. extractionthe resulting mixture is extracted into methylene chloride
  6. customThe extracts are dried
  7. concentrationconcentrated
  8. customthe solid residue is recrystallized

출처 및 근거

ORD 기록
ord-790e922d1c994de495aaa4e1d41b6c16
출처 데이터셋
uspto-grants-1978_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04073912

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