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Sulfuric Acid → 2-methyl-9-methoxy-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one

HRID 1448517
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HRID 1448517 반응식
[CH2:1]([C:4]1[CH:5]=[C:6]2[C:11](=[C:12]([O:15][CH3:16])[C:13]=1[OH:14])[O:10][C:9](=[O:17])[CH:8]=[CH:7]2)[CH:2]=[CH2:3].S(=O)(=O)(O)O>>[CH3:3][CH:2]1[O:14][C:13]2=[C:12]([O:15][CH3:16])[C:11]3[O:10][C:9](=[O:17])[CH:8]=[CH:7][C:6]=3[CH:5]=[C:4]2[CH2:1]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 1118Sulfuric AcidHCID 218145006-Allyl-7-hydroxy-8-methoxycoumarin

생성물 1

HCID 203802232-methyl-9-methoxy-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one

실험 절차

A sample of 1.0 g. (4.31 mmoles) of 6-allyl-7-hydroxy-8-methoxycoumarin was dissolved in 20 ml. of conc. sulfuric acid at 25°. After 10 min, the solution was diluted with ice water. The mixture was extracted with methylene chloride, dried over sodium sulfate, and evaporated to yield 90 g. of residue. This was filtered through a column of silica gel, eluting with benzene/ethyl acetate, 4:1, to afford, upon evaporation of the filtrate, pure 2-methyl-9-methoxy-2,3-dihydro-7H-furo[3,2-g][1]benzopyran-7-one as a white solid. Recrystallization from ethanol yielded an analytical sample, mp 115°-116°.

후처리

  1. customat 25°
  2. extractionThe mixture was extracted with methylene chloride
  3. dry with material
dried over sodium sulfate
  • customevaporated
  • customto yield 90 g
  • filtrationThis was filtered through a column of silica gel
  • washeluting with benzene/ethyl acetate, 4:1
  • 출처 및 근거

    ORD 기록
    ord-3b7ed2c0dbc743299b6a029e4606b795
    출처 데이터셋
    uspto-grants-1979_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04180659

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