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Hydrogen Peroxide → 2-Carboxy-6-chloropyridine 1-oxide

HRID 481308
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반응식

HRID 481308 반응식
[Cl:1][C:2]1[N:7]=[C:6]([C:8]([OH:10])=[O:9])[CH:5]=[CH:4][CH:3]=1.[OH:11]O>FC(F)(F)C(O)=O>[Cl:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]([C:8]([OH:10])=[O:9])[N+:7]=1[O-:11]
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참가 물질

4

반응물 2

HCID 784Hydrogen PeroxideHCID 208126-Chloropicolinic acid

생성물 1

HCID 536813382-Carboxy-6-chloropyridine 1-oxide수율 67%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

To a solution of 6-chloro-2-pyridinecarboxylic acid (14.8 g, 0.093 mol, for preparation, see Delarge, II. Farmaco-Ed.Sc., 1967, 22, 1069) in trifluoroacetic acid (110 ml) was added 75 ml of 30% aqueous hydrogen peroxide solution. The mixture was heated to 60° for 2 hours, cooled to room temperature and poured onto ice water. The white precipitate was filtered and was washed well with water to yield 10.8 g (67%) of the title compound of this preparation. mp 168°-170° C. 1H NMR (CDCl3): δ 7.46 (1H, d, J=8), 7.77 (1H, dd, J=8, 8), 8.01 (1H, d, J=8).

후처리

  1. temperatureThe mixture was heated to 60° for 2 hours
  2. additionpoured onto ice water
  3. filtrationThe white precipitate was filtered
  4. washwas washed well with water
  5. customto yield

출처 및 근거

ORD 기록
ord-19fb74ca5ccc480c85a1d82d3c14c559
출처 데이터셋
uspto-grants-1998_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05789408

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