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3,4-Dimethoxybenzonitrile → 3,4-Dimethoxythiobenzamide

HRID 1489229
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HRID 1489229 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[C:6]#[N:7].C(N)(=[S:15])C>Cl.CN(C=O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[C:6]([NH2:7])=[S:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 748423,4-DimethoxybenzonitrileHCID 2723949Thioacetamide

생성물 1

HCID 27584903,4-Dimethoxythiobenzamide수율 61.9%

시약·촉매·용매 1

HCID 10920465N,N-dimethylformamide;hydrochloride용매

반응 조건

온도
90 °C

실험 절차

25 g of 3,4-dimethoxybenzonitrile and 23 g of thioacetamide were dissolved in 120 ml of 10% hydrochloric acid-DMF. The solution was heated at 90° C. for 3 hours. The solution was further heated at 130° C. for 5 hours to conduct a reaction. The solvent was removed by distillation. The residue was washed twice with 100 ml of diethyl ether. Similar washing was conducted with 100 ml of water. The resulting crystals were collected by filtration and dried. Recrystallization from methanol was conducted to obtain 18.7 g of 3,4-dimethoxythiobenzamide as light brown columnar crystals.

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후처리

  1. temperatureThe solution was further heated at 130° C. for 5 hours
  2. customa reaction
  3. customThe solvent was removed by distillation
  4. washThe residue was washed twice with 100 ml of diethyl ether
  5. washSimilar washing
  6. filtrationThe resulting crystals were collected by filtration
  7. customdried
  8. customRecrystallization from methanol

출처 및 근거

ORD 기록
ord-0d15f9812a7349fe9a037f20fa86f756
출처 데이터셋
uspto-grants-1997_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05677319

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