Sodium ethoxide → HCID 68515561, Verbindung

Ethyl 5-methyl-3-oxo-4-hexenoate (1.10 g, 6.56 mmol, 1.1 eq.) obtained in Example 95a) and 4-azido-N-ethylbenzamide (purity 90%, 1.23 g, 5.82 mmol) were dissolved in ethanol (25 ml), sodium ethoxide (550 mg, 7.82 mmol, 1.25 eq.) was added, and the mixture was stirred at room temperature for 30 min and at 50° C. for 10.5 hr. Ethanol was evaporated from the reaction mixture, and the residue was diluted with 2% aqueous sodium carbonate solution (40 ml) and washed with ethyl acetate (40 ml). The organic layer was extracted with 2% aqueous sodium carbonate solution (15 ml). The aqueous layers were combined, washed with ethyl acetate-hexane (2:1, 50 ml), acidified (pH<3) with 6N hydrochloric acid and extracted three times with ethyl acetate (50 ml) and ethyl acetate-THF (3:1, 40 ml). The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated, and ethyl acetate was added. The precipitate was collected by filtration, washed with ethyl acetate and diethyl ether and dried to give the title compound as a grayish white powder (1.43 g, 4.55 mmol, 78.2%).

1. customEthanol was evaporated from the reaction mixture
2. additionthe residue was diluted with 2% aqueous sodium carbonate solution (40 ml)
3. washwashed with ethyl acetate (40 ml)
4. extractionThe organic layer was extracted with 2% aqueous sodium carbonate solution (15 ml)
5. washwashed with ethyl acetate-hexane (2:1, 50 ml)
6. extractionextracted three times with ethyl acetate (50 ml) and ethyl acetate-THF (3:1, 40 ml)
7. washwashed with saturated brine
8. dry with materialdried over anhydrous sodium sulfate
9. concentrationconcentrated
10. additionethyl acetate was added
11. filtrationThe precipitate was collected by filtration
12. washwashed with ethyl acetate and diethyl ether
13. customdried

ORD-Eintrag

ord-b87e60d71d604214bc6a8beced7c9519

Quelldatensatz

uspto-grants-2010_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07803822B2