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Sodium Hydroxide → 3-(Methanesulfonylmethyl)aniline

HRID 1633950
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HRID 1633950 반응식
[CH3:1][S:2]([CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-])=O)[CH:7]=1)(=[O:4])=[O:3].[OH-].[Na+]>C(O)C>[CH3:1][S:2]([CH2:5][C:6]1[CH:7]=[C:8]([CH:9]=[CH:10][CH:11]=1)[NH2:12])(=[O:3])=[O:4]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 179084331-(Methanesulfonylmethyl)-3-nitrobenzene

생성물 1

HCID 219563393-(Methanesulfonylmethyl)aniline수율 55.2%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

1-Methylsulfonylmethyl-3-nitrobenzene (4.70 g, 21.8 mmol) was added ethanol (70 mL) and the mixture was heated to reflux. At reflux the mixture was added SnCl2 dihydrate (24.6 g, 109 mmol) and heating at reflux was continued for 1 hour. After cooling, the mixture was poured into ice/water (200 mL) and neutralised (to pH 7) with 1 N sodium hydroxide. The mixture was filtered through celite, and the filter cake was washed with ethyl acetate. The phases from the combined filtrate and washings were separated, and the aqueous phase was extracted with ethyl acetate (2×150 mL). The combined organic phases were dried (MgSO4) and evaporated in vacuo to afford 2.23 g (55%) 3-(methylsulfonylmethyl)aniline.

후처리

  1. temperaturethe mixture was heated to reflux
  2. temperatureAt reflux the mixture
  3. temperatureheating
  4. temperatureat reflux
  5. temperatureAfter cooling
  6. filtrationThe mixture was filtered through celite
  7. washthe filter cake was washed with ethyl acetate
  8. customThe phases from the combined filtrate and washings were separated
  9. extractionthe aqueous phase was extracted with ethyl acetate (2×150 mL)
  10. dry with materialThe combined organic phases were dried (MgSO4)
  11. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-419d725560d445c3b988c21c79631844
출처 데이터셋
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06503949B1

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