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Sodium Hydroxide → 3-(Methanesulfonylmethyl)aniline

HRID 1633950
ノート
印刷プレビュー

反応式

HRID 1633950 の反応式
[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]
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 14798Sodium HydroxideHCID 179084331-(Methanesulfonylmethyl)-3-nitrobenzene

生成物 1

HCID 219563393-(Methanesulfonylmethyl)aniline収率 55.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-419d725560d445c3b988c21c79631844
出典データセット
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06503949B1

反応ノート

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