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Acetic Acid → 1-Phenyl-4-(cyclohexyl-sulfinyl)-5-chloropyridazin-6-one

HRID 620135
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반응식

HRID 620135 반응식
OO.[C:3]1([N:9]2[C:14](=[O:15])[C:13]([Cl:16])=[C:12]([S:17][CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)[CH:11]=[N:10]2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C(O)(=[O:26])C>O>[C:3]1([N:9]2[C:14](=[O:15])[C:13]([Cl:16])=[C:12]([S:17]([CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)=[O:26])[CH:11]=[N:10]2)[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 784Hydrogen PeroxideHCID 132094401-Phenyl-4-(cyclohexylthio)-5-chloropyridazin-6-one

생성물 1

HCID 132094411-Phenyl-4-(cyclohexyl-sulfinyl)-5-chloropyridazin-6-one

시약·촉매·용매 1

HCID 962Water용매

실험 절차

5.1 parts by volume of 30% strength by weight hydrogen peroxide were added dropwise to a solution of 16 parts by weight of 1-phenyl-4-(cyclohexylthio)-5-chloropyridazin-6-one in 100 parts by volume of glacial acetic acid, and stirring was continued for 12 hours at 60° C. The reaction mixture was then stirred into 1,000 parts by volume of water, and the precipitate was filtered off under suction, washed with water and dried under reduced pressure. 16.3 parts by weight of 1-phenyl-4-(cyclohexyl-sulfinyl)-5-chloropyridazin-6-one of melting point 128°-130° C. were obtained (compound No.1).

후처리

  1. filtrationthe precipitate was filtered off under suction
  2. washwashed with water
  3. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-baf2a870b9c5475b8f30640d976a63dc
출처 데이터셋
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04820704

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