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Methylamine → 3-bromo-N-methylbenzene-1-sulfonamide

HRID 78320
ノート
印刷プレビュー

反応式

HRID 78320 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([S:8](Cl)(=[O:10])=[O:9])[CH:5]=[CH:6][CH:7]=1.[CH3:12][NH2:13]>C1COCC1>[CH3:12][NH:13][S:8]([C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([Br:1])[CH:3]=1)(=[O:10])=[O:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6329MethylamineHCID 17943m-Bromobenzenesulphonyl chloride

生成物 1

HCID 72132653-bromo-N-methylbenzene-1-sulfonamide収率 100%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 3-bromobenzenesulfonyl chloride (2.5 g, 11.2 mmol) in THF (15 mL) at 0° C. was added methylamine (2.0 M in THF; 28 mL, 56 mmol). The resulting solution was allowed to warm to room temp. and was stirred at room temp. overnight. The resulting mixture was separated between EtOAc (25 mL) and a 1 M HCl solution (25 mL). The aqueous phase was back-extracted with EtOAc (2×25 mL). The combined organic phases were sequentially washed with water (2×25 mL) and a saturated NaCl solution (25 mL), dried (MgSO4) and concentrated under reduced pressure to give N-methyl-3-bromobenzenesulfonamide as a white solid (2.8 g, 99%).

後処理

  1. temperatureto warm to room temp.
  2. customThe resulting mixture was separated between EtOAc (25 mL)
  3. extractionThe aqueous phase was back-extracted with EtOAc (2×25 mL)
  4. washThe combined organic phases were sequentially washed with water (2×25 mL)
  5. dry with materiala saturated NaCl solution (25 mL), dried (MgSO4)
  6. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-1c8365b710764efca9fb600eaa2c80d1
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08841330B2

反応ノート

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