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Methanol → Methyl 4-chloro-2-methoxy-5-nitrobenzoate

HRID 1059295
ノート
印刷プレビュー

反応式

HRID 1059295 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([O:14][CH3:15])[C:5](=[CH:9][C:10]=1[N+:11]([O-:13])=[O:12])[C:6]([OH:8])=[O:7].S(=O)(=O)(O)O.[CH3:21]O>>[Cl:1][C:2]1[CH:3]=[C:4]([O:14][CH3:15])[C:5](=[CH:9][C:10]=1[N+:11]([O-:13])=[O:12])[C:6]([O:8][CH3:21])=[O:7]
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 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 128487494-Chloro-2-methoxy-5-nitrobenzoic acid

生成物 1

HCID 18670222Methyl 4-chloro-2-methoxy-5-nitrobenzoate

実験手順

To a solution of 3.1 g of 4-chloro-5-nitro-o-anisic acid in methanol (100 ml) was added a catalytic amount of sulfuric acid and the resulting mixture was heated under reflux for 3 hours. Then the reaction mixture was poured into ice/water and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. After distilling off the solvent under reduced pressure, 3.3 g of methyl 4-chloro-5-nitro-o-anisate was obtained as pale yellow crystals.

後処理

  1. temperaturethe resulting mixture was heated
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
  • temperatureunder reflux for 3 hours
  • extractionextracted with ethyl acetate
  • washThe organic layer was washed with a saturated aqueous solution of sodium chloride
  • dry with materialdried over anhydrous magnesium sulfate
  • distillationAfter distilling off the solvent under reduced pressure
  • 出典と根拠

    ORDレコード
    ord-67639995a53349839fff77166b274da7
    出典データセット
    uspto-grants-2003_02
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06518423B1

    反応ノート

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