Sulfuric Acid → Oxazolo[4,5-b]pyridin-2-yl(phenyl)methanone

HRID 259541노트

반응식

HRID 259541 반응식
[CH2:1]([C:8]1[O:9][C:10]2[C:11]([N:16]=1)=[N:12][CH:13]=[CH:14][CH:15]=2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Mn]([O-])(=O)(=O)=[O:18].[K+].S(=O)(=O)(O)O.S(=O)(O)[O-].[Na+]>[OH-].[Na+].O>[C:1]([C:8]1[O:9][C:10]2[C:11]([N:16]=1)=[N:12][CH:13]=[CH:14][CH:15]=2)(=[O:18])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

참가 물질

7

실험 절차

A mixture of 800 mg. of 2-benzyloxazolo[ 4,5-b]pyridine, 2.5 g. of potassium permanganate, 35 ml. of water and 6 drops of 2.5 N sodium hydroxide solution was heated at 50°-55° C. for 3 hours. After cooling, sulfuric acid was added to about pH 6 and sufficient sodium bisulfite was added to remove the manganese dioxide. The crystalline precipitate remaining was collected and recrystallized from ethylacetate to give 2-benzoyloxazolo[ 4,5-b]pyridine, m.p. 151°-153° C.

후처리

  1. additionA mixture of 800 mg
  2. temperatureAfter cooling
  3. additionwas added
  4. customto remove the manganese dioxide
  5. customThe crystalline precipitate remaining was collected
  6. customrecrystallized from ethylacetate

출처 및 근거

ORD 기록
ord-64d993bda4cc4700b6fea06edea0ec03
출처 데이터셋
uspto-grants-1977_07
특허 번호
US04038396

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