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Dimethylformamide → HCID 19806696, 화합물

HRID 1681466
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HRID 1681466 반응식
[CH2:1]([O:3][C:4]1[C:8]([Cl:9])=[C:7](Cl)[S:6][N:5]=1)[CH3:2].[CH3:11][S:12][O-:13].[Na+].CN(C=[O:19])C>C(OCC)C>[CH2:1]([O:3][C:4]1[C:8]([Cl:9])=[C:7]([S:12]([CH3:11])(=[O:19])=[O:13])[S:6][N:5]=1)[CH3:2]
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참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 19806678HCID 19806678, 화합물HCID 23717576HCID 23717576, 화합물

생성물 1

HCID 19806696HCID 19806696, 화합물

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

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온도
100 °C

실험 절차

To a solution of 3-ethoxy-4,5-dichloroisothiazole (19.8 g, 0.10 mol) in DMF (50 ml) under a nitrogen atmosphere was added sodium methanesulfenate (20.4 g, 0.20 mol). The mixture was warmed to 100° C. and stirred for two days. The reaction mixture was then cooled, diluted with diethyl ether, washed with water, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The residue was chromatographed on a silica gel column, eluting with chloroform, to give 7.1 g of the title compound, mp 85°-87° , crystallized from cyclohexane. A by-product, 3-ethoxy-4,5-bis(methylsulfonyl)isothiazole (3.9 g) was also obtained, mp 158°-160° (crystallized from cyclohexane).

후처리

  1. temperatureThe reaction mixture was then cooled
  2. washwashed with water
  3. dry with materialdried over anhydrous sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe residue was chromatographed on a silica gel column
  7. washeluting with chloroform

출처 및 근거

ORD 기록
ord-26c8de8e610746339adcc9475d618aed
출처 데이터셋
uspto-grants-1992_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05171860

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