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4-Chloro-4'-methylbutyrophenone → 2-[1-(4-Methyl-phenyl)-4-chloro-butylidene]-hydrazinecarbothioamide

HRID 613687
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HRID 613687 반응식
[NH2:1][NH:2][C:3]([NH2:5])=[S:4].[Cl:6][CH2:7][CH2:8][CH2:9][C:10]([C:12]1[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=1)=O>CO.Cl.O>[CH3:18][C:15]1[CH:16]=[CH:17][C:12]([C:10](=[N:1][NH:2][C:3](=[S:4])[NH2:5])[CH2:9][CH2:8][CH2:7][Cl:6])=[CH:13][CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 987454-Chloro-4'-methylbutyrophenoneHCID 2723789Thiosemicarbazide

생성물 1

HCID 541274022-[1-(4-Methyl-phenyl)-4-chloro-butylidene]-hydrazinecarbothioamide수율 75.2%

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매HCID 887Methanol용매HCID 962Water
용매

실험 절차

Thiosemicarbazide (6.84 g, 75 mmol) was added under nitrogen to a solution of 4-chloro-4'-methylbutyrophenone (10.0 g, 50 mmol) in 175 mL of methanol plus 13.5 mL of 1 N HCl plus 12.5 mL of water and the reaction stirred at room temperature overnight. The solid formed was collected by filtration and dissolved in methylene chloride. The organic solution was washed multiple times with water, dried (MgSO4) and the solvent removed under reduced pressure to give 10.15 g of an off-white solid. Recrystallization of the solid from isopropyl alcohol gave 8.65 g (64%) of the tide compound as an off-white solid, mp133-135° C.

후처리

  1. customThe solid formed
  2. filtrationwas collected by filtration
  3. dissolutiondissolved in methylene chloride
  4. washThe organic solution was washed multiple times with water
  5. dry with materialdried (MgSO4)
  6. customthe solvent removed under reduced pressure

출처 및 근거

ORD 기록
ord-5f1abbbe2bbd47828c907cf2310e5e60
출처 데이터셋
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06008362

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