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N,N-Dimethylaniline → 3-(Dimethylamino)benzene-1-sulfonyl chloride

HRID 641899
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HRID 641899 반응식
[S:1]([Cl:5])(=O)(=[O:3])[OH:2].[CH3:6][N:7]([CH3:14])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1>ClCCl>[CH3:6][N:7]([CH3:14])[C:8]1[CH:9]=[C:10]([S:1]([Cl:5])(=[O:3])=[O:2])[CH:11]=[CH:12][CH:13]=1
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참가 물질

4

반응물 2

HCID 949N,N-DimethylanilineHCID 24638Chlorosulfonic acid

생성물 1

HCID 534147043-(Dimethylamino)benzene-1-sulfonyl chloride수율 11.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
0 °C

실험 절차

Sulfurochloridic acid (100 g, 862.07 mmol) was cooled to 0° C. and N,N-dimethylbenzenamine (20 g, 165.29 mmol) was added dropwise with stirring, maintaining a temperature of 0° C. The resulting solution was then heated to 120° C. and stirred for 3 hours. After cooling to room temperature, dichloromethane (40 mL) was added and the resulting mixture was added dropwise to 100 mL of ice/salt water. The resulting solution was extracted with dichloromethane (3×500 mL) and the organic layers combined, dried (Na2SO4) and filtered. The filtrate was concentrated and the residue was purified by column chromatography using a 1:100 ethyl acetate/petroleum ether solvent system. The collected fractions were combined and concentrated to give 4.1 g (11%) of 3-(dimethylamino) benzene-1-sulfonyl chloride as a yellow solid. 1H NMR (CDCl3) δ 7.41 (t, 1H), 7.31 (d, 1H), 7.23 (s, 1H), 6.98 (m, 1H), 3.05 (s, 6H).

후처리

  1. temperatureThe resulting solution was then heated to 120° C.
  2. stirringstirred for 3 hours
  3. temperatureAfter cooling to room temperature
  4. extractionThe resulting solution was extracted with dichloromethane (3×500 mL)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated
  8. customthe residue was purified by column chromatography
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-4d938b0c917b4dff89a252b9fe590690
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07696229B2

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