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

HRID 256605
ノート
印刷プレビュー

反応式

HRID 256605 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-0533d51cf27c41d48af9351d24ce8f58
出典データセット
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05258399

反応ノート

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