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

HRID 337614
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HRID 337614 반응식
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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

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

생성물 1

HCID 668959895-Bromo-2,3-dimethylbenzoic acid

시약·촉매·용매 2

HCID 24470Silver Nitrate촉매HCID 962
Water
용매
2회

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-37e33c4d6ec0494685f67ce10f914856
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889714B2

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