반응식
[CH3:1][C:2]([C:4]1[CH:5]=[CH:6][C:7]([OH:10])=[CH:8][CH:9]=1)=[O:3].[O:11]1CCOCC1>O>[OH:10][C:7]1[CH:8]=[CH:9][C:4]([C:2]([CH:1]=[O:11])=[O:3])=[CH:5][CH:6]=1참가 물질
4
실험 절차
4-Hydroxyacetophenone (15 g., 0.11 mol) was dissolved in 70 ml. dioxane and 8.3 ml. H2O. SeO2 (12.2 g., 0.11 mol) was added and the mixture heated at 80° for 18 hours, then filtered over diatomaceous earth. The filtrate was stripped, taken up in 150 ml. H2O, heated on a steam bath, decolorized with activated carbon, cooled to refrigerator temperature, and hydrate of title product recovered by filtration, 5.72 g. Anhydrous title product was obtained by Kugelrohr distillation; 1H-nmr 5.97 (s, 1H), 6.97 (d, 2H, J=6 Hz), 8.22 (d, 2H, J=6 Hz), 9.68 (s, 1H).
후처리
- temperaturethe mixture heated at 80° for 18 hours
- filtrationfiltered over diatomaceous earth
- temperatureH2O, heated on a steam bath
- temperaturecooled to refrigerator temperature, and hydrate of title product
- filtrationrecovered by filtration, 5.72 g
출처 및 근거
- ORD 기록
- ord-0bd1ed2d172f4f46b6de2cd7c4b5dd26
- 출처 데이터셋
- uspto-grants-1988_08
- 특허 번호
- US04762921
연결된 노트
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