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Sodium Nitrite → Ethyl 6-hydroxybenzo[d]isoxazole-3-carboxylate

HRID 424637
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HRID 424637 반응식
N[C:2]1[CH:15]=[CH:14][C:5]2[C:6]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[N:7][O:8][C:4]=2[CH:3]=1.N([O-])=[O:17].[Na+]>S(=O)(=O)(O)O.O.[N+]([O-])([O-])=O.[Cu+2].[N+]([O-])([O-])=O.[Cu-]=O>[OH:17][C:2]1[CH:15]=[CH:14][C:5]2[C:6]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[N:7][O:8][C:4]=2[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 2

HCID 23668193Sodium NitriteHCID 57355978Ethyl 6-aminobenzo[d]isoxazole-3-carboxylate

생성물 1

HCID 136216618Ethyl 6-hydroxybenzo[d]isoxazole-3-carboxylate수율 99%

시약·촉매·용매 4

HCID 18616Cupric nitrate촉매HCID 178419072HCID 178419072, 화합물촉매HCID 962
Water
용매
3회
HCID 1118Sulfuric Acid용매

실험 절차

Ethyl 6-aminobenzo[d]isoxazole-3-carboxylate (2.43 mmol) was diluted with a solution of sulfuric acid (2.5 mL) in water (2.5 mL) and the resulting mixture was maintained at rt for 30 min. A solution of sodium nitrite (2.67 mmol) in water (2.5 ml) was added dropwise at 0° C. and the resulting mixture was maintained for 30 min at 0° C. This aqueous solution was added to a cold (0° C.) solution of copper (II) nitrate (149 mmol) in water (80 mL) and the reaction mixture was allowed to warm to rt. After 5 min., copper (I) oxide (2.78 mmol) was added to the mixture and the reaction mixture was maintained for 1 h at rt. The reaction mixture was extracted with ethyl acetate (3×100 mL) and the combined organic layers were dried (magnesium sulfate) and concentrated to provide crude ethyl 6-hydroxybenzo[d]isoxazole-3-carboxylate in 99% yield as a brown oil.

후처리

  1. temperaturethe resulting mixture was maintained for 30 min at 0° C
  2. temperatureto warm to rt
  3. temperaturethe reaction mixture was maintained for 1 h at rt
  4. extractionThe reaction mixture was extracted with ethyl acetate (3×100 mL)
  5. dry with materialthe combined organic layers were dried (magnesium sulfate)
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-1e63a6fec163400da8771ee4e39e7b56
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08106066B2

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