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Sulfuryl chloride → 4-Chloro-2,3-dihydro-1,2-benzothiazol-3-one

HRID 502608
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HRID 502608 반응식
[Cl:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([S:11]C)[C:3]=1/[CH:4]=[N:5]/O.S(Cl)(Cl)(=O)=[O:14]>C1(C)C=CC=CC=1>[Cl:1][C:2]1[C:3]2[C:4](=[O:14])[NH:5][S:11][C:7]=2[CH:8]=[CH:9][CH:10]=1
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참가 물질

4

반응물 2

HCID 24648Sulfuryl chlorideHCID 17910216(NE)-N-[(2-chloro-6-methylsulfanylphenyl)methylidene]hydroxylamine

생성물 1

HCID 574365604-Chloro-2,3-dihydro-1,2-benzothiazol-3-one

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
80 °C

실험 절차

(E)-2-Chloro-6-(methylthio)benzaldehyde oxime (12.37 g) was dissolved in toluene (35 mL). Sulfuryl chloride (5.4 ml, 66.24 mmol) was added, dropwise to the solution at 0° C., followed by heating at 80° C. for 1 h. After the completion of the reaction, the reaction mixture was cooled to room temperature and a white precipitate formed. The solid was collected by vacuum filtration, washed with toluene and air dried to 4-chlorobenzo[d]isothiazol-3(2H)-one (6 g). (This method is general for other 2-(methythio) benzaldehyde oximes.) 1H NMR (300 MHz, DMSO-d6): 7.90 (t, 1H), 7.55 (t, 1H), 7.41 ppm (d, 1H). MW=186 confirmed by LC-MS, tr=2.38 min (Method B) MH+=187.

후처리

  1. customAfter the completion of the reaction
  2. temperaturethe reaction mixture was cooled to room temperature
  3. customa white precipitate formed
  4. filtrationThe solid was collected by vacuum filtration
  5. washwashed with toluene and air
  6. dry with materialdried to 4-chlorobenzo[d]isothiazol-3(2H)-one (6 g)
  7. customconfirmed by LC-MS, tr=2.38 min (Method B) MH+=187

출처 및 근거

ORD 기록
ord-dfacf1a4ce5644e48c25069af136a072
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07776847B2

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