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Lawesson's reagent → 2-Methylfuran-3-carbothioamide

HRID 1416550
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반응식

HRID 1416550 반응식
[CH3:1][C:2]1[O:3][CH:4]=[CH:5][C:6]=1[C:7]([NH2:9])=O.C(=O)(O)[O-].[Na+].COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:24])=CC=1>C1(C)C=CC=CC=1>[CH3:1][C:2]1[O:3][CH:4]=[CH:5][C:6]=1[C:7](=[S:24])[NH2:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 87949Lawesson's reagentHCID 516892Sodium BicarbonateHCID 107729742-Methylfuran-3-carboxamide

생성물 1

HCID 126012172-Methylfuran-3-carbothioamide

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A reaction mixture of N-[4-chloro-3-[dimethylhydrazono)methyl]phenyl]-2-methyl 3-furancarboxamide (1 g), sodium bicarbonate (1.8 g) and Lawesson's reagent (0.9 g) in toluene (20 mL) was refluxed for 3 hours. The reaction mixture was then cooled and filtered through a plug of neutral aluminum oxide and eluted with ether. Evaporation of the solvent produced 0.6 g of N-[4-chloro-3-[dimethylhydrazono)methyl]phenyl]-2-methyl-3-furancarbothioamide, m.p. 90-92° C.

후처리

  1. temperaturewas refluxed for 3 hours
  2. temperatureThe reaction mixture was then cooled
  3. filtrationfiltered through a plug of neutral aluminum oxide
  4. washeluted with ether
  5. customEvaporation of the solvent

출처 및 근거

ORD 기록
ord-cc3e6aa34502418fa51a4f9eb4ec3adf
출처 데이터셋
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05914351

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