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Chloroform → 3-Tosyloxy-2,2-dimethyl-1-propanesulfonamide

HRID 1590057
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반응식

HRID 1590057 반응식
[OH:1][CH2:2][C:3]([CH3:10])([CH3:9])[CH2:4][S:5]([NH2:8])(=[O:7])=[O:6].[C:11]1([CH3:21])[CH:16]=[CH:15][C:14]([S:17](Cl)(=[O:19])=[O:18])=[CH:13][CH:12]=1.C(Cl)(Cl)Cl>N1C=CC=CC=1>[S:17]([O:1][CH2:2][C:3]([CH3:10])([CH3:9])[CH2:4][S:5]([NH2:8])(=[O:7])=[O:6])([C:14]1[CH:15]=[CH:16][C:11]([CH3:21])=[CH:12][CH:13]=1)(=[O:19])=[O:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6212ChloroformHCID 73974-Toluenesulfonyl chlorideHCID 103296873-Hydroxy-2,2-dimethylpropane-1-sulfonamide

생성물 1

HCID 100646893-Tosyloxy-2,2-dimethyl-1-propanesulfonamide수율 88.4%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To a solution of 5.0 g of 3-hydroxy-2,2-dimethyl-1-propanesulfonamide in 18 ml of pyridine was added 6.3 g of p-toluenesulfonyl chloride under ice-cooling and stirring. After 2 hours, the reaction mixture was poured into a mixture of 300 ml of chloroform and 100 ml of ice-water. The separated chloroform layer was washed in turn with diluted hydrochloric acid and water, dried over anhydrous magnesium sulfate and distilled under reduced pressure to obtain 8.5 g of 3-tosyloxy-2,2-dimethyl-1-propanesulfonamide.

후처리

  1. temperaturecooling
  2. washThe separated chloroform layer was washed in turn with diluted hydrochloric acid and water
  3. dry with materialdried over anhydrous magnesium sulfate
  4. distillationdistilled under reduced pressure

출처 및 근거

ORD 기록
ord-66c8ad8b776a49c2b623497482845fa6
출처 데이터셋
uspto-grants-1993_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05202324

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