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Acetone → HCID 22621002、化合物

HRID 430429
ノート
印刷プレビュー

反応式

HRID 430429 の反応式
[CH3:1]I.[CH3:3][C:4]1[CH:12]=[CH:11]C(C(O)=O)=[C:6]([NH:13][S:14]([CH3:17])(=[O:16])=[O:15])[CH:5]=1.[C:18](=[O:21])([O-])[O-].[K+].[K+].C[C:25]([CH3:27])=[O:26]>>[CH3:3][C:4]1[CH:12]=[CH:11][C:27]([C:25]([O:21][CH3:18])=[O:26])=[C:6]([N:13]([CH3:1])[S:14]([CH3:17])(=[O:15])=[O:16])[CH:5]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 180AcetoneHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 22620944HCID 22620944、化合物

生成物 1

HCID 22621002HCID 22621002、化合物

実験手順

Methyl iodide (22.0 ml) was added to a stirred suspension of 4-methyl-2-(N-methylsulphonylamino)benzoic acid (8.0 g) and anhydrous potassium carbonate (24.2 g) in acetone and the mixture was stirred and heated at reflux overnight. The mixture was cooled and filtered and the filtrate was evaporated to dryness. The residue was dissolved in dichloromethane and washed with aqueous sodium bicarbonate solution, water, dried (magnesium sulphate) and filtered. The filtrate was evaporated to dryness to give methyl 4-methyl-2-(N-methyl-N-methylsulphonylamino)benzoate (8.36 g) as a cream solid, m.p. 100-103° C.

後処理

  1. temperatureheated
  2. temperatureat reflux overnight
  3. temperatureThe mixture was cooled
  4. filtrationfiltered
  5. customthe filtrate was evaporated to dryness
  6. dissolutionThe residue was dissolved in dichloromethane
  7. washwashed with aqueous sodium bicarbonate solution, water
  8. dry with materialdried (magnesium sulphate)
  9. filtrationfiltered
  10. customThe filtrate was evaporated to dryness

出典と根拠

ORDレコード
ord-9bea601e4f6d4f1cae3f909694faf4ac
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06323155B1

反応ノート

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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