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Thionyl Chloride → HCID 13772106, 화합물

HRID 1380478
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HRID 1380478 반응식
[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10]([O-:13])(=O)=[O:11])=[CH2:3].[K+].S(Cl)([Cl:17])=O>CN(C)C=O>[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10]([Cl:17])(=[O:13])=[O:11])=[CH2:3]
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 23687389HCID 23687389, 화합물

생성물 1

HCID 13772106HCID 13772106, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A mixture of potassium 2-(1-methylethenyl)benzenesulfonate (7.8 g, 0.33 mmol) and 30 ml of thionyl chloride was contacted with 1.5 ml of N,N-dimethylformamide at 0°. The mixture was allowed to warm to room temperature over 45 minutes then evaporated in vacuo. Water and ether were added and the aqueous phase extracted with several portions of ether. The combined ether layers were washed with saturated sodium chloride solution, dried and evaporated under reduced pressure to yield the title compound as an oil.

후처리

  1. customthen evaporated in vacuo
  2. additionWater and ether were added
  3. extractionthe aqueous phase extracted with several portions of ether
  4. washThe combined ether layers were washed with saturated sodium chloride solution
  5. customdried
  6. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-469ba4a6c6144a20ab6ff39dc0090f16
출처 데이터셋
uspto-grants-1986_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04582525

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