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

HRID 1771702
ノート
印刷プレビュー

反応式

HRID 1771702 の反応式
[CH3:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[N+]([O-])(O)=O.[Br:16]Br>C(O)(=O)C.O.[N+]([O-])([O-])=O.[Ag+]>[Br:16][C:8]1[CH:9]=[C:10]([CH3:11])[C:2]([CH3:1])=[C:3]([CH:7]=1)[C:4]([OH:6])=[O:5]
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 3

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

生成物 1

HCID 668959895-Bromo-2,3-dimethylbenzoic acid収率 83.9%

試薬・触媒・溶媒 3

HCID 24470Silver Nitrate触媒HCID 176Acetic Acid溶媒
HCID 962
Water
溶媒
2 回

実験手順

To a solution of 2,3-dimethylbenzoic acid (5 g, 33.3 mmol, 1.0 eq) in acetic acid (167 mL) at room temperature was added a solution of conc. nitric acid (25.2 g, 399 mmol, 12 eq), water (15 g, 0.83 mmol, 25 eq) and bromine (5.85 g, 36.6 mmol, 1.1 eq). A solution of silver nitrate (7.35 g, 43 mmol, 1.3 eq) in water (43 mL) was then added dropwise over 30 min. Once addition was completed, the reaction was stirred at room temperature for 1 h, then quenched by addition of water and EtOAc. The aqueous layer was extracted with EtOAc and the combined organic extracts were washed with water and brine, dried (Na2SO4), filtered and evaporated in vacuo to give the title compound as a yellow solid (6.4 g, 83%).

後処理

  1. additionOnce addition
  2. customquenched by addition of water and EtOAc
  3. extractionThe aqueous layer was extracted with EtOAc
  4. washthe combined organic extracts were washed with water and brine
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. customevaporated in vacuo

出典と根拠

ORDレコード
ord-00b35b8177a041dfb08c39923f514293
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09249085B2

反応ノート

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