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Sodium hydroxide methanol → Sodium 5-(m-chlorobenzylsulfinyl)-2-pyridinecarboxylate

HRID 259248
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인쇄 미리보기

반응식

HRID 259248 반응식
C[O:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([S:11]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([Cl:20])[CH:15]=2)=[O:12])=[CH:7][N:6]=1)=[O:4].CO.[OH-].[Na+:24]>>[Cl:20][C:16]1[CH:15]=[C:14]([CH:19]=[CH:18][CH:17]=1)[CH2:13][S:11]([C:8]1[CH:9]=[CH:10][C:5]([C:3]([O-:4])=[O:2])=[N:6][CH:7]=1)=[O:12].[Na+:24]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 23721981Sodium hydroxide methanolHCID 537728025-(m-Chlorobenzylsulfinyl)-2-pyridinecarboxylic acid methyl ester

생성물 1

HCID 23712206Sodium 5-(m-chlorobenzylsulfinyl)-2-pyridinecarboxylate

실험 절차

To the stirred mixture of 9 g of 5-(m-chlorobenzylsulfinyl)-2-pyridinecarboxylic acid methyl ester and 40 ml of N aqueous sodium hydroxide methanol is added until dissolution occurs. The solution is heated at the steam bath for 10 minutes and stirred overnight at room temperature. It is evaporated, the residue taken up in the minimum amount of hot water, the solution filtered, the filtrate cooled and the precipitate formed collected, to yield the sodium 5-(m-chlorobenzylsulfinyl)-2-pyridinecarboxylate.

후처리

  1. additionis added until dissolution
  2. temperatureThe solution is heated at the steam bath for 10 minutes
  • customIt is evaporated
  • filtrationthe solution filtered
  • temperaturethe filtrate cooled
  • customthe precipitate formed
  • customcollected
  • 출처 및 근거

    ORD 기록
    ord-8193c3a539c04da494a76533be71fa8b
    출처 데이터셋
    uspto-grants-1977_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04036965

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