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Carbon Tetrachloride → 2-CHLORO-1-(m-NITROPHENYLSULFONYL)ETHYL PHENYL SULFIDE

HRID 1156374
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HRID 1156374 반응식
[CH:1]([S:3]([C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[CH:7]=1)(=[O:5])=[O:4])=[CH2:2].[C:15]1([S:21]Cl)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.C(Cl)(Cl)(Cl)[Cl:24]>C(O)(=O)C>[C:15]1([S:21][CH:1]([S:3]([C:6]2[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[CH:7]=2)(=[O:4])=[O:5])[CH2:2][Cl:24])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 5943Carbon TetrachlorideHCID 11008040Benzenesulfenyl chlorideHCID 20535994HCID 20535994, 화합물

생성물 1

HCID 130447962-CHLORO-1-(m-NITROPHENYLSULFONYL)ETHYL PHENYL SULFIDE

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

In a mixture of 50 ml of glacial acetic acid and 100 ml of carbon tetrachloride at 56° was dissolved 30.9 g (0.145 mole) of m-nitrophenyl vinyl sulfone. Addition of 21.0 g (0.145 mole) of benzenesulfenyl chloride produced an exotherm to 58°. The clear solution was allowed to stand for seventy hours. Removal of the solvent by evaporation at reduced pressure and recrystallization of the residue from toluene gave yellow needles, m.p. 125.5°-126.5°.

후처리

  1. customproduced an exotherm to 58°
  2. waitto stand for seventy hours
  3. customRemoval of the solvent
  4. customby evaporation
  5. customat reduced pressure and recrystallization of the residue from toluene
  6. customgave yellow needles, m.p. 125.5°-126.5°

출처 및 근거

ORD 기록
ord-d86eb5f1d56041bca1589d18bb349d69
출처 데이터셋
uspto-grants-1982_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04335142

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