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Triethylamine → N-(2-Chloro-4-methylphenyl)methanesulfonamide

HRID 256605
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HRID 256605 반응식
[Cl:1][C:2]1[CH:8]=[C:7]([CH3:9])[CH:6]=[CH:5][C:3]=1[NH2:4].C(N(CC)CC)C.[CH3:17][S:18](Cl)(=[O:20])=[O:19]>ClCCl>[Cl:1][C:2]1[CH:8]=[C:7]([CH3:9])[CH:6]=[CH:5][C:3]=1[NH:4][S:18]([CH3:17])(=[O:20])=[O:19]
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 120072-Chloro-p-toluidineHCID 31297Methanesulfonyl chloride

생성물 1

HCID 19785609N-(2-Chloro-4-methylphenyl)methanesulfonamide수율 32.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 2-chloro-4-methylaniline (5.00 g) and triethylamine (3.57 g) in dichloromethane (100 ml) was cooled to 0° C. Methanesulphonyl chloride (4.04 g) was added dropwise and the mixture stirred at ambient temperature overnight. The mixture was then washed with 2N aqueous hydrochloric acid solution (50 ml) and the solvent removed by evaporation. The residue was dissolved in ethyl acetate (75 ml) extracted with 2N aqueous sodium hydroxide solution (2×50 ml). The aqueous phase was acidified with 2N aqueous hydrochloric acid solution and extracted with ethyl acetate (2×75 ml). This was subsequently dried (MgSO4) and the solvent evaporated. Thus was obtained N-(2-chloro-4-methylphenyl)methanesulphonamide (2.5 g, 32%). NMR Spectrum 2.33 (3H, s), 2.97 (3H, s), 6.6 (1H, s), 7.10 (1H, d), 7.25 (1H, s), 7.52 (1H, d).

후처리

  1. washThe mixture was then washed with 2N aqueous hydrochloric acid solution (50 ml)
  2. customthe solvent removed by evaporation
  3. dissolutionThe residue was dissolved in ethyl acetate (75 ml)
  4. extractionextracted with 2N aqueous sodium hydroxide solution (2×50 ml)
  5. extractionextracted with ethyl acetate (2×75 ml)
  6. dry with materialThis was subsequently dried (MgSO4)
  7. customthe solvent evaporated

출처 및 근거

ORD 기록
ord-0533d51cf27c41d48af9351d24ce8f58
출처 데이터셋
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05258399

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