Cesium carbonate → 2-(2-Methoxy-4-(methoxycarbonyl)phenoxy)propanoic acid

Temperatur

100 °C

Methyl 4-hydroxy-3-methoxybenzoate (1.09 g, 5.98 mmol) and tert-butyl 2-bromopropanoate (1.25 g, 0.97 mL, 5.98 mmol) and cesium carbonate (1.95 g, 5.98 mmol) were added into DMF (10 mL) in a 20 mL microwave vial equipped with a stir bar and sealed. The mixture was heated in Biotage microwave synthesizer for 1 hour at 100° C. The solvent was removed and the remained sticky oil was dissolved in DCM (7 mL) and TFA (7 mL). The mixture was stirred overnight. The reaction mixture was neutralized with sodium bicarbonate and organic layer was separated from the mixture. The aqueous layer was washed with DCM (2×10 mL), combined organics and acidified to around pH5 with 2N HCl. Aqueous was extracted with DCM and then with ethyl acetate, dried with sodium sulfate and concentrated to an oil. The crude product was dissolved in DCM (4 mL) and a pure product (0.530 g) precipitate out from the solution by adding diethyl ether (4 mL).

1. customvial equipped with a stir bar
2. customsealed
3. customThe solvent was removed
4. dissolutionthe remained sticky oil was dissolved in DCM (7 mL)
5. customwas separated from the mixture
6. washThe aqueous layer was washed with DCM (2×10 mL)
7. extractionAqueous was extracted with DCM
8. dry with materialwith ethyl acetate, dried with sodium sulfate
9. concentrationconcentrated to an oil
10. dissolutionThe crude product was dissolved in DCM (4 mL)
11. customa pure product (0.530 g) precipitate out from the solution
12. additionby adding diethyl ether (4 mL)

ORD-Eintrag

ord-0e608b891ab74f639964008fff45563a

Quelldatensatz

uspto-grants-2010_06

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07745463B2