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Nitric Acid → Methyl 2-(4-chloro-3-nitrophenyl)-2-methylpropionate

HRID 352384
ノート
印刷プレビュー

反応式

HRID 352384 の反応式
[N+:1]([O-:4])(O)=[O:2].S(=O)(=O)(O)O.[Cl:10][C:11]1[CH:16]=[CH:15][C:14]([C:17]([CH3:23])([CH3:22])[C:18]([O:20][CH3:21])=[O:19])=[CH:13][CH:12]=1>>[Cl:10][C:11]1[CH:12]=[CH:13][C:14]([C:17]([CH3:23])([CH3:22])[C:18]([O:20][CH3:21])=[O:19])=[CH:15][C:16]=1[N+:1]([O-:4])=[O:2]
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 944Nitric AcidHCID 1118Sulfuric AcidHCID 22709436Methyl 2-(4-chlorophenyl)-2-methylpropanoate

生成物 1

HCID 22709425Methyl 2-(4-chloro-3-nitrophenyl)-2-methylpropionate収率 100%

実験手順

After dropwise addition of 40.0 g of concentrated nitric acid to 90.7 g of concentrated sulfuric acid under ice cooling, 62.3 g of methyl 2-(4-chlorophenyl)-2-methylpropionate was added dropwise. The resulting mixture was stirred at room temperature for 30 minutes. The reaction mixture was poured into ice water, followed by extraction with ethyl acetate. The organic layer was washed successively with water and brine, dried over anhydrous sodium sulfate and evaporated under reduced pressure, whereby 75.5 g of the title compound was obtained.

後処理

  1. extractionfollowed by extraction with ethyl acetate
  2. washThe organic layer was washed successively with water and brine
  3. dry with materialdried over anhydrous sodium sulfate
  4. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-b500b76b8e7f44c3b311539eb0c3d430
出典データセット
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06747022B2

反応ノート

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