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Methyl iodide → HCID 178503870, 화합물

HRID 1578044
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HRID 1578044 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[NH:9][C:10]([NH:12][C:13](=[O:15])[CH3:14])=[S:11].[C:16](=O)([O-])[O-].[Na+].[Na+].CI>CC(C)=O>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[NH:9][C:10](=[N:12][C:13](=[O:15])[CH3:14])[S:11][CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 10340Sodium CarbonateHCID 12952276HCID 12952276, 화합물

생성물 1

HCID 178503870HCID 178503870, 화합물

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

5.2 g (0.02 M) of N-(2,6-dichlorophenyl)-N'-acetylthiourea, 1.3 g (0.012 M) of sodium carbonate, 1.5 ml (0.024 M) of methyliodide and 200 ml of acetone are boiled under energetic shaking for 10 hours. The acetone is distilled off and the residue is washed and then filtered. After drying 4.9 g (88.5% from the theoretical yield of N-(2,6-dichlorophenyl)-N'-acetyl-S-methylisothiourea are obtained with a melting point 135-139° C. After recrystallization from ethanol, the melting point of the product is 139°-141° C.

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후처리

  1. distillationThe acetone is distilled off
  2. washthe residue is washed
  3. filtrationfiltered
  4. dry with materialAfter drying 4.9 g (88.5% from the theoretical yield of N-(2,6-dichlorophenyl)-N'-acetyl-S-methylisothiourea
  5. customare obtained with a melting point 135-139° C
  6. customAfter recrystallization from ethanol
  7. customis 139°-141° C.

출처 및 근거

ORD 기록
ord-207bfb9d804d4a9da38fb504ac678b71
출처 데이터셋
uspto-grants-1981_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04290971

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