Ethyl benzoylacetate → 4-Penten-1-one, 1-phenyl-

Ethyl benzoylacetate (38.4 g, 0.2 mole, Aldrich) was added to a mixture of sodium ethoxide (13.6 g, 0.2 moles) in 200 mL ethanol. The mixture was stirred magnetically and slowly brought to reflux. After 30 minutes, the reaction mixture was cooled and allyl bromide (26.6 g, 0.22 moles, Aldrich) was added via a syringe with care (10 minutes), and the mixture was refluxed for another 2 hours. After cooling to room temperature, the mixture was transferred to a separatory funnel and diluted with 300 mL saturated sodium bicarbonate and extracted with ether (200 mL×3). The combined ether layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was removed by rotary evaporation resulting in a brownish oil. Without further purification, the crude product was suspended in 250 mL 1 normal sodium hydroxide solution and brought to gentle reflux overnight. After cooling, the oil that floated on top was separated and was combine with the organic layer from the extractions that followed. The aqueous layer was acidified with 50% sulfuric acid to pH 1 and heated to reflux for 5 hours. The mixture was extracted with ethyl acetate (200 mL×3). The organic layer was dried over sodium sulfate and the solvent removed by rotary evaporation to yield a yellow oil. Yield: 19.7 g (61.5%) with boiling point 70-80° C. at 0.8 mmHg. 1H-NMR (CDCl3, δ): phenyl ring (7.97, d, 2H, 7.55, m, 1H, 7.4, m, 2H); vinyl group (5.8, m 2H, 5.1 q, 1H); 3.08 (t, 2H); 2.5 (m, 2H). See also, Vogel et al., Vogel's Textbook of Practical Organic Chemistry. Fifth Edition, revised by Furniss et al., 1989, Pearson Prentice Hall).

1. temperatureto reflux
2. temperaturethe reaction mixture was cooled
3. temperaturethe mixture was refluxed for another 2 hours
4. customthe mixture was transferred to a separatory funnel
5. extractionextracted with ether (200 mL×3)
6. washThe combined ether layer was washed with brine
7. dry with materialdried over anhydrous magnesium sulfate
8. customThe solvent was removed by rotary evaporation
9. customresulting in a brownish oil
10. customWithout further purification
11. temperatureto gentle reflux overnight
12. temperatureAfter cooling
13. customwas separated
14. extractionfrom the extractions that
15. temperatureheated
16. temperatureto reflux for 5 hours
17. extractionThe mixture was extracted with ethyl acetate (200 mL×3)
18. dry with materialThe organic layer was dried over sodium sulfate
19. customthe solvent removed by rotary evaporation
20. customto yield a yellow oil

ORDレコード

ord-43980f5e70bc49998f8042c4c9e29387

出典データセット

uspto-grants-2010_06

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07741375B2