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Thionyl Chloride → (4-Methylphenyl)methanesulfonyl chloride

HRID 971389
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HRID 971389 반응식
[CH3:1][C:2]1[CH:12]=[CH:11][C:5]([CH2:6][S:7]([O-])(=[O:9])=[O:8])=[CH:4][CH:3]=1.[Na+].S(Cl)([Cl:16])=O>CN(C)C=O>[CH3:1][C:2]1[CH:12]=[CH:11][C:5]([CH2:6][S:7]([Cl:16])(=[O:9])=[O:8])=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 23665764HCID 23665764, 화합물

생성물 1

HCID 2794648(4-Methylphenyl)methanesulfonyl chloride

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
-10 °C

실험 절차

In dimethylformamide (90 ml) is dispersed sodium p-methylbenzylsulfonate (30 g, 0.145 mol) which is sufficientry dry. The dispersion is cooled to -10° C. and under stirring, thionyl chloride (19.2 ml, 0.29 mol) is added dropwise. The mixture is stirred at room temperature for 3 hours and poured in ice-water (500 g) and extracted with ether (3 times, 150 ml each). The ethereal layers are combined, washed twice with cold water and dried over sodium sulfate. The ether is distilled off and petroleum ether is added to the crystalline residue, followed by cooling. The crystals are collected by filtration.

후처리

  1. stirringThe mixture is stirred at room temperature for 3 hours
  2. extractionextracted with ether (3 times, 150 ml each)
  3. washwashed twice with cold water
  4. dry with materialdried over sodium sulfate
  5. distillationThe ether is distilled off
  6. additionpetroleum ether is added to the crystalline residue
  7. temperatureby cooling
  8. filtrationThe crystals are collected by filtration

출처 및 근거

ORD 기록
ord-d96c483122954d13aca8149095237097
출처 데이터셋
uspto-grants-1979_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04159979

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