반응식
[C:1]1([CH3:9])[CH:6]=[CH:5][C:4]([CH:7]=O)=[CH:3][CH:2]=1.[OH-].[Na+].O.C(OCC)(=O)C.[CH3:19][C:20]([CH3:22])=[O:21]>>[C:1]1([CH3:9])[CH:6]=[CH:5][C:4]([CH:7]=[CH:19][C:20](=[O:21])[CH3:22])=[CH:3][CH:2]=1참가 물질
6
실험 절차
In a 250 ml single neck flask was charged 12.1 g (100 mmoles,1.0 eq) of p-tolualdehyde dissolved in 30 ml of acetone. To this was added 5 g of 10% aqueous sodium hydroxide solution (12.5 mmoles, 0.125 eq), dropwise and during the course of addition, temperature was kept no higher than 25° C., while the mixture was agitated continuously for 30 minutes. To the mixture was added 50 ml of water, followed by 100 ml of ethyl acetate, the phases were separated and the organic phase was washed with water three times and then dried, and concentrated to obtain 13.5 g of 4-(p-tolyl)-3-buten-2-one as a faintly yellow oil in 84.3% yield.
후처리
- additiondropwise and during the course of addition, temperature
- customwas kept no higher than 25° C., while the mixture
- customthe phases were separated
- washthe organic phase was washed with water three times
- customdried
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-2316b2d1c5d945f09eb0457f01df58c8
- 출처 데이터셋
- uspto-grants-2001_01
- 특허 번호
- US06177462B1
연결된 노트
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