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Acetic Acid → 5-Bromo-2,3-dimethylbenzoic acid

HRID 337614
ノート
印刷プレビュー

反応式

HRID 337614 の反応式
C(O)(=O)C.[CH3:5][C:6]1[C:14]([CH3:15])=[CH:13][CH:12]=[CH:11][C:7]=1[C:8]([OH:10])=[O:9].[N+]([O-])(O)=O.[Br:20]Br>O.[N+]([O-])([O-])=O.[Ag+]>[Br:20][C:12]1[CH:13]=[C:14]([CH3:15])[C:6]([CH3:5])=[C:7]([CH:11]=1)[C:8]([OH:10])=[O:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 176Acetic AcidHCID 944Nitric AcidHCID 117822,3-Dimethylbenzoic acidHCID 24408Bromine

生成物 1

HCID 668959895-Bromo-2,3-dimethylbenzoic acid

試薬・触媒・溶媒 2

HCID 24470Silver Nitrate触媒HCID 962
Water
溶媒
2 回

実験手順

To a stirred acetic acid solution (0.2 M) of 2,3-dimethylbenzoic acid (1 eq.) was added sequentially nitric acid (12 eq.), water (25 eq.) and bromine (1.1 eq.). Finally, silver nitrate (1 M aqueous solution, 1.3 eq.) was added dropwise over a period of 30 min. After another hour of stirring at RT, the crude reaction mixture was diluted with water and extracted with EtOAc. The combined organic extracts were then washed with brine, dried over Na2SO4, filtered and the filtrate concentrated in vacuo. Trituration of the crude product thus obtained in hexanes afforded the title compound as a yellow solid.

後処理

  1. customthe crude reaction mixture
  2. extractionextracted with EtOAc
  3. washThe combined organic extracts were then washed with brine
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. concentrationthe filtrate concentrated in vacuo
  7. customTrituration of the crude product thus obtained in hexanes

出典と根拠

ORDレコード
ord-37e33c4d6ec0494685f67ce10f914856
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08889714B2

反応ノート

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