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2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran → 3,4-dihydro-2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran

HRID 892504
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HRID 892504 반응식
[CH3:1][C:2]1([CH3:18])[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=2)[C:5]2[CH:14]=[CH:15][CH:16]=[CH:17][C:4]=2[O:3]1.[H][H]>C(O)C.[Pd]>[CH3:1][C:2]1([CH3:18])[CH2:7][CH:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=2)[C:5]2[CH:14]=[CH:15][CH:16]=[CH:17][C:4]=2[O:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 187551522,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyranHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 198956113,4-dihydro-2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran수율 72.3%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

6.95 g of 2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran were dissolved in 100 ml of ethanol and shaken at room temperature with 10% palladium-on-charcoal under a hydrogen atmosphere. After the required volume of hydrogen had been taken up the catalyst was filtered off, the filtrate was evaporated and the residue was recrystallized from n-hexane to give 5.07 g of 3,4-dihydro-2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran of melting point 99°-101° C.

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후처리

  1. filtrationwas filtered off
  2. customthe filtrate was evaporated
  3. customthe residue was recrystallized from n-hexane

출처 및 근거

ORD 기록
ord-b50302337b7d45c28953d17a540f89b9
출처 데이터셋
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05118694

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