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Dimethylamine → 5-chloro-N,N-dimethylpentane-1-sulfonamide

HRID 565735
ノート
印刷プレビュー

反応式

HRID 565735 の反応式
[CH3:1][NH:2][CH3:3].[Cl:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][S:10](Cl)(=[O:12])=[O:11]>C(OCC)C>[CH3:1][N:2]([CH3:3])[S:10]([CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][Cl:4])(=[O:12])=[O:11]
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 674DimethylamineHCID 12589202HCID 12589202、化合物

生成物 1

HCID 221115315-chloro-N,N-dimethylpentane-1-sulfonamide収率 95.1%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

A 50% aqueous solution of dimethylamine (5.95 g, 66 mmol) was added dropwise to a solution of diethyl ether (60 ml) and 5-chloropentanesulfonyl chloride (6.15 g, 30 mmol) with stirring under ice-cooling. Thereafter, the mixture was stirred at the same temperature for 20 minutes. The reaction solution was washed twice with water (10 ml) and then with brine (10 ml), and thereafter dried over anhydrous magnesium sulfate. Subsequently, the solvent was removed by evaporation in vacuo. The crude product was purified by column chromatography on silica gel with ethyl acetate-n-hexane (1:4), to give N,N-dimethyl-5-chloropentanesulfonamide (6.10 g) as a pale yellow oil.

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. temperaturecooling
  2. stirringThereafter, the mixture was stirred at the same temperature for 20 minutes
  3. washThe reaction solution was washed twice with water (10 ml)
  4. dry with materialwith brine (10 ml), and thereafter dried over anhydrous magnesium sulfate
  5. customSubsequently, the solvent was removed by evaporation in vacuo
  6. customThe crude product was purified by column chromatography on silica gel with ethyl acetate-n-hexane (1:4)

出典と根拠

ORDレコード
ord-c85b37a9dc244bc096ca2b8a93c0a7eb
出典データセット
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06172228B2

反応ノート

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