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3,4-Dichloro-2-methyl-5-ethoxycarbonylisothiazolium fluorosulfonate → 4-Chloro-5-ethoxycarbonyl-2-methyl-4-isothiazolin-3-one

HRID 1278378
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HRID 1278378 반응식
FS([O-])(=O)=[O:3].Cl[C:7]1[C:11]([Cl:12])=[C:10]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[S:9][N+:8]=1[CH3:18]>C([O-])([O-])=O.[K+].[K+]>[Cl:12][C:11]1[C:7](=[O:3])[N:8]([CH3:18])[S:9][C:10]=1[C:13]([O:15][CH2:16][CH3:17])=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 128890133,4-Dichloro-2-methyl-5-ethoxycarbonylisothiazolium fluorosulfonate

생성물 1

HCID 128890594-Chloro-5-ethoxycarbonyl-2-methyl-4-isothiazolin-3-one수율 37.6%

시약·촉매·용매 1

HCID 11430Potassium Carbonate용매

실험 절차

3,4-Dichloro-5-ethoxycarbonyl-2-methylisothiazolium fluorosulfonate (4.2 g, 0.012 mol) was added to 50 ml of saturated K2CO3 solution. The aqueous phase was extracted with 3×50 ml of CH2Cl2. Then combined extracts were dried (MgSO4), filtered and conc. to yield a solid. Recrystallization from heptane yielded 1.0 g (35%) of 4-chloro-5-ethoxycarbonyl-2-methyl-4-isothiazolin-3-one, mp 142-147.

후처리

  1. extractionThe aqueous phase was extracted with 3×50 ml of CH2Cl2
  2. dry with materialThen combined extracts were dried (MgSO4)
  3. filtrationfiltered
  4. customconc. to yield a solid
  5. customRecrystallization from heptane

출처 및 근거

ORD 기록
ord-21f276798cbe472f9feee595215a9664
출처 데이터셋
uspto-grants-1981_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04281136

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