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3,5-Dinitroperbenzoic acid → 3-Methoxy-4-bromoisothiazole-1-oxide

HRID 1681474
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HRID 1681474 반응식
[CH3:1][O:2][C:3]1[C:7]([Br:8])=[CH:6][S:5][N:4]=1.[N+](C1C=C([N+]([O-])=O)C=C(C(OO)=O)C=1)([O-])=[O:10]>C(Cl)Cl>[CH3:1][O:2][C:3]1[C:7]([Br:8])=[CH:6][S:5](=[O:10])[N:4]=1
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참가 물질

4

반응물 2

HCID 101769383,5-Dinitroperbenzoic acidHCID 123939314-Bromo-3-methoxy-1,2-thiazole

생성물 1

HCID 198066893-Methoxy-4-bromoisothiazole-1-oxide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 3-methoxy-4-bromoisothiazole (2.9 g, 15 mmol) in methylene chloride (15 ml) there can be was added, in portions, 3,5-dinitroperbenzoic acid (3.4 g, 15 mmol) with ice bath cooling. After about one hour, the precipitated 3,5-dinitrobenzoic acid can be filtered off and the solvent evaporated in vacuo. By triturating the residue with diethyl ether, a crystalline product, 3-methoxy-4-bromoisothiazole-1-oxide, can be obtained. Additional material can be obtained by chromatographing the mother liquors on silica gel, eluting with chloroform.

후처리

  1. temperaturecooling
  2. filtrationthe precipitated 3,5-dinitrobenzoic acid can be filtered off
  3. customthe solvent evaporated in vacuo
  4. customBy triturating the residue with diethyl ether

출처 및 근거

ORD 기록
ord-8193099e661c4196a7bab6f9bfbe0c85
출처 데이터셋
uspto-grants-1992_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05171860

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