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Diethyl Ether → 2-(2,2-dimethyl-2H-1-benzopyran-4-yl)pyridine N-oxide

HRID 1073888
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HRID 1073888 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.ClC1C=CC=C(C(OO)=[O:27])C=1.C(OCC)C>ClCCl>[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[O-:27])[C:5]2[CH:14]=[CH:15][CH:16]=[CH:17][C:4]=2[O:3]1
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참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 70297m-Chloroperbenzoic acidHCID 187551522,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran

생성물 1

HCID 543388622-(2,2-dimethyl-2H-1-benzopyran-4-yl)pyridine N-oxide수율 2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

1.61 g of 2,2-dimethyl-4-(2-pyridyl)-2H-1-benzopyran were dissolved in 10 ml of dichloromethane at room temperature and 2.0 g of m-chloroperbenzoic acid were added. After 1 hour the mixture was washed with sodium bisulphite solution, sodium bicarbonate solution and water. The organic phase was dried over sodium sulphate and evaporated. The residue was chromatographed on silica gel using ethyl acetate/ethanol/formic acid (40:4:1) for the elution. The product was obtained as an oil which solidified upon trituration with diethyl ether. Recrystallization from toluene gave 0.034 g of 2-(2,2-dimethyl-2H-1-benzopyran-4-yl)pyridine N-oxide of melting point 148-150° C.

후처리

  1. washAfter 1 hour the mixture was washed with sodium bisulphite solution, sodium bicarbonate solution and water
  2. dry with materialThe organic phase was dried over sodium sulphate
  3. customevaporated
  4. customThe residue was chromatographed on silica gel
  5. washfor the elution
  6. customThe product was obtained as an oil which
  7. customRecrystallization from toluene

출처 및 근거

ORD 기록
ord-7cf01dd28f6441ffbaee0449f5a07c3c
출처 데이터셋
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04971982

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