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

HRID 565735
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HRID 565735 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 674DimethylamineHCID 12589202HCID 12589202, 화합물

생성물 1

HCID 221115315-chloro-N,N-dimethylpentane-1-sulfonamide수율 95.1%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

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.

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후처리

  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)

출처 및 근거

ORD 기록
ord-c85b37a9dc244bc096ca2b8a93c0a7eb
출처 데이터셋
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06172228B2

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