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Hydrogen Peroxide → 6-Fluoroquinoxaline-2-carboxylic acid

HRID 2302074
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HRID 2302074 반응식
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([CH:12]=[O:13])[CH:6]=[N:5]2.[OH:14]O>C(O)=O.Cl>[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([C:12]([OH:14])=[O:13])[CH:6]=[N:5]2
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참가 물질

5

반응물 2

HCID 784Hydrogen PeroxideHCID 221364416-Fluoroquinoxaline-2-carbaldehyde

생성물 1

HCID 221364266-Fluoroquinoxaline-2-carboxylic acid수율 45%

시약·촉매·용매 2

HCID 284Formic Acid용매HCID 313Hydrochloric Acid용매

실험 절차

Using the method of Dodd (Synthesis, 1993, 295-297), a solution of 6-fluoroquinoxaline-2-carboxaldehyde (71 mg, 0.4 mmol) in formic acid (2 mL) was cooled in an ice bath and treated with hydrogen peroxide (2 mL of 30%). The reaction was stirred in the ice bath for 3 hours. After this time the reaction mixture was diluted with 10% HCl (25 mL) and extracted with dichloromethane (4×25 mL). The combined organic extracts were dried over anhydrous MgSO4, filtered and concentrated to afford 35 mg (45%) of 6-fluoroquinoxaline-2-carboxylic acid.

후처리

  1. customthe method of Dodd (Synthesis, 1993, 295-297)
  2. extractionextracted with dichloromethane (4×25 mL)
  3. dry with materialThe combined organic extracts were dried over anhydrous MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-6caf66a7d6734dce80b64684beeac523
출처 데이터셋
uspto-grants-2002_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06429207B1

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