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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Chlorobenzene → Benzene, 1,1'-sulfonylbis-, dichloro deriv.

HRID 2351106
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인쇄 미리보기

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HRID 2351106 반응식
Cl[S:2]([OH:5])(=O)=[O:3].S(Cl)(Cl)=O.[Cl:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>>[CH:15]1[CH:16]=[C:11]([Cl:10])[CH:12]=[C:13]([S:2]([C:13]2[CH:14]=[CH:15][CH:16]=[C:11]([Cl:10])[CH:12]=2)(=[O:5])=[O:3])[CH:14]=1
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참가 물질

4

반응물 3

HCID 7964ChlorobenzeneHCID 24386Thionyl ChlorideHCID 24638Chlorosulfonic acid

생성물 1

HCID 3037034Benzene, 1,1'-sulfonylbis-, dichloro deriv.수율 197.3%

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온도
195 °C

실험 절차

The filtrate from Example 1 is freed from methoanol by distillation, the residue is returned to the reaction vessel, and 562.5 g (5 mol) of chlorobenzene is added. chlorobenzenesulfonic acid chloride is formed by adding 476 g (4 mol) of chlorosulfonic acid and 466 g (4 mol) of thionyl chloride, the mixture is heated to 195° C., and 337.5 g (3 mol) of chlorobenzene is added at such a rate that the temperature does not fall. the charge is subsequently treated as described in Example 1, giving 850 g (74% yield) of dichlorodiphenyl sulfone of melting point 149°-150° C. Gas-chromatographic analysis of the product gives 99.6% 4,4'-isomer, 0.3% 2,4'-isomer, and 0.1% 3,4'-isomer.

후처리

  1. additionthe charge is subsequently treated

출처 및 근거

ORD 기록
ord-cefd6b2212304d3691e1ad736c296592
출처 데이터셋
uspto-grants-1989_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04871876

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