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Chlorosulfonyl isocyanate → 4-(3,4-Dichlorophenyl)azetidin-2-one

HRID 430071
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HRID 430071 반응식
ClS([N:5]=[C:6]=[O:7])(=O)=O.[Cl:8][C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][C:16]=1[Cl:17])[CH:12]=[CH2:13]>C(OCC)C>[Cl:8][C:9]1[CH:10]=[C:11]([CH:12]2[NH:5][C:6](=[O:7])[CH2:13]2)[CH:14]=[CH:15][C:16]=1[Cl:17]
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참가 물질

4

반응물 2

HCID 70918Chlorosulfonyl isocyanate2회HCID 748693,4-Dichlorostyrene

생성물 1

HCID 183537284-(3,4-Dichlorophenyl)azetidin-2-one

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

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온도
70 °C

실험 절차

To chlorosulfonyl isocyanate (CSI) (2.46 ml) in diethyl ether (8 ml) was added dropwise with stirring 3,4-dichlorostyrene (4.89 g, 28.3 mmol). The reaction was heated to 35° C. for 90 min after which time a further 1 ml CSI was added. The reaction was left for 16 h at 35° C., then the oil bath temperature was increased to 70° C. and the ether distilled off. The reaction was stirred at 70° C. for 1 h then cooled and slurried in dichloromethane (50 ml), and added portionwise with stirring to water containing sodium bisulfite (10 g) and potassium carbonate (15 g), using an ice bath for cooling. After stirring for 30 min. the phases were separated and the organic phase dried (MgSO4) to give a yellow oil (4 g). Purification by column chromatography on silica gel eluting with 0-50% dichloromethane in hexane gave the title compound as a white solid, (2.6 g, 43%). δH (CDCl3) 2.85 (1H, dd), 3.45 (1H, m), 4.7 (1H, m), 6.35 (1H, bs), 7.25 (1H, m), 7.45 (2H, m).

후처리

  1. additionwas added
  2. distillationthe ether distilled off
  3. temperaturethen cooled
  4. additionadded portionwise
  5. stirringwith stirring to water
  6. additioncontaining sodium bisulfite (10 g) and potassium carbonate (15 g)
  7. temperaturefor cooling
  8. stirringAfter stirring for 30 min. the phases
  9. customwere separated
  10. dry with materialthe organic phase dried (MgSO4)

출처 및 근거

ORD 기록
ord-47725bb1b490446ca904faac382a425c
출처 데이터셋
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06320051B1

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