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Water → N-[(2,3-Dihydro-1H-inden-2-yl)carbamothioyl]benzamide

HRID 1287895
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HRID 1287895 반응식
[S-:1][C:2]#[N:3].[NH4+].[C:5](Cl)(=[O:12])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[NH2:14][CH:15]1[CH2:23][C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH2:16]1.O>CC(C)=O>[C:5]([NH:3][C:2]([NH:14][CH:15]1[CH2:23][C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH2:16]1)=[S:1])(=[O:12])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 7412Benzoyl chlorideHCID 15666Ammonium thiocyanateHCID 763102-Aminoindane

생성물 1

HCID 21507070N-[(2,3-Dihydro-1H-inden-2-yl)carbamothioyl]benzamide수율 72.6%

시약·촉매·용매 1

HCID 180Acetone용매3회

실험 절차

To a stirred solution of ammonium thiocyanate (0.837 g.) in acetone (5 ml.) was added benzoyl chloride (1.406 g.) in acetone (10 ml.). The mixture was refluxed for 5 minutes then 2-aminoindane (1.332 g.) in acetone (10 ml.) was added quickly. Refluxing was continued for 10 minutes and the mixture poured into water (75 ml.) to give an oil which solidified on standing. Recrystallisation from ethanol/water afforded the title compound as pale yellow needles (2.151 g.), m.p. 130°-5° C.

후처리

  1. temperatureThe mixture was refluxed for 5 minutes
  2. temperatureRefluxing
  3. customto give an oil which
  4. customRecrystallisation from ethanol/water

출처 및 근거

ORD 기록
ord-2818b60ef8164b189d5ffba3fcc91c5a
출처 데이터셋
uspto-grants-1976_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03985898

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