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Triethylamine → N-(2-iodophenyl)methanesulfonamide

HRID 985718
ノート
印刷プレビュー

反応式

HRID 985718 の反応式
[CH3:1][S:2](Cl)(=[O:4])=[O:3].[I:6][C:7]1[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=1[NH2:9].C(N(CC)CC)C>ClCCl>[I:6][C:7]1[CH:13]=[CH:12][CH:11]=[CH:10][C:8]=1[NH:9][S:2]([CH3:1])(=[O:4])=[O:3]
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 119952-IodoanilineHCID 31297Methanesulfonyl chloride

生成物 1

HCID 780001N-(2-iodophenyl)methanesulfonamide収率 75.4%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

Methanesulfonyl chloride (4.4 mL, 57 mmol) was added to a 0° C. dichloromethane (200 mL) solution containing 2-iodoaniline (5.0 g, 23 mmol) and triethylamine (9.6 mL, 69 mmol). The resulting mixture was stirred for 90 minutes, washed with HCl (0.5 M). The organics were separated then dried over sodium sulfate and concentrated in vacuo. The residue was then treated with potassium hydroxide (2.0 M in 1:1 methanol:water, 75 mL) for 30 min. This material was then diluted with dichloromethane and washed with HCl (1.0 N, 300 mL). The organics were separated then dried over sodium sulfate and concentrated to provide the title compound (5.15 g) as a tan solid.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. washwashed with HCl (0.5 M)
  2. customThe organics were separated
  3. dry with materialthen dried over sodium sulfate
  4. concentrationconcentrated in vacuo
  5. additionThe residue was then treated with potassium hydroxide (2.0 M in 1:1 methanol:water, 75 mL) for 30 min
  6. additionThis material was then diluted with dichloromethane
  7. washwashed with HCl (1.0 N, 300 mL)
  8. customThe organics were separated
  9. dry with materialthen dried over sodium sulfate
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-6a22d669e1cf487c81ae823682ef95a2
出典データセット
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06872834B2

反応ノート

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