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3,4-dihydro-2H-pyrano[2,3-c]pyridin-6-ylmethanol → 3,4-dihydro-2H-pyrano[2,3-c]pyridine-6-carbaldehyde

HRID 1510685
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HRID 1510685 반응식
[O:1]1[C:6]2=[CH:7][N:8]=[C:9]([CH2:11][OH:12])[CH:10]=[C:5]2[CH2:4][CH2:3][CH2:2]1>C(Cl)(Cl)Cl.[O-2].[O-2].[Mn+4]>[O:1]1[C:6]2=[CH:7][N:8]=[C:9]([CH:11]=[O:12])[CH:10]=[C:5]2[CH2:4][CH2:3][CH2:2]1
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참가 물질

4

반응물 1

HCID 223133613,4-dihydro-2H-pyrano[2,3-c]pyridin-6-ylmethanol

생성물 1

HCID 566403113,4-dihydro-2H-pyrano[2,3-c]pyridine-6-carbaldehyde수율 97.2%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 6212Chloroform용매

실험 절차

To a solution of 0.25 g of (3,4-dihydro-2H-pyrano(2,3-c)pyridin-6-yl)methanol in 7.5 mL of chloroform, 0.66 g of manganese dioxide was added, and the mixture was heated under reflux while stirring for 4 hours 50 minutes. The reaction mixture was cooled to room temperature, the insoluble substance was then filtered off, and the solvent was distilled off under reduced pressure to obtain 0.24 g of 3,4-dihydro-2H-pyrano(2,3-c)pyridine-6-carbaldehyde as a light yellow oily substance.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux
  3. filtrationthe insoluble substance was then filtered off
  4. distillationthe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-5bcfa702ed5f4ae4bfda8e29be2cfcdc
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08211908B2

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