Trifluoroacetic acid → N-{4-[2-(4-Methoxyphenyl)ethoxy]benzoyl}glycine

Temperatur

100 °C

(Tributyl phosphoranylidene)acetonitrile (428 μL, 1.50 mmol) was added to a solution of toluene (7 mL) containing N-(4-hydroxybenzoyl)glycine tert-butyl ester (264 mg, 1.05 mmol) prepared in Example 1 (1a) and 2-(4-methoxyphenyl)ethanol (176 mg, 1.16 mmol). The mixture was stirred at 100° C. for 3.5 hours, and then water was added thereto. The mixture was extracted with ethyl acetate. The organic layers were combined, washed with water and saturated brine, and dried over anhydrous magnesium sulfate. Then, the solvent was evaporated. The resulting residue was purified by silica gel column chromatography (hexane to hexane:ethyl acetate, 6:1, 4:1, and 3:1, v/v) to give an oily substance (358 mg). To a solution of dichloromethane (1 mL) containing this oily substance (358 mg, 0.929 mmol), trifluoroacetic acid (0.5 mL) was added. The mixture was stirred at room temperature for 1 hour, and then the solvent was evaporated. Diisopropyl ether was added to the resulting residue to suspend it. The produced precipitate was collected by filtration and was washed with diisopropyl ether to give 248 mg of the title compound (colorless crystalline solid, yield: 72%).

1. extractionThe mixture was extracted with ethyl acetate
2. washwashed with water and saturated brine
3. dry with materialdried over anhydrous magnesium sulfate
4. customThen, the solvent was evaporated
5. customThe resulting residue was purified by silica gel column chromatography (hexane to hexane
6. customethyl acetate, 6:1, 4:1, and 3:1, v/v) to give an oily substance (358 mg)
7. additionwas added
8. stirringThe mixture was stirred at room temperature for 1 hour
9. customthe solvent was evaporated
10. additionDiisopropyl ether was added to the resulting residue
11. filtrationThe produced precipitate was collected by filtration
12. washwas washed with diisopropyl ether

ORD-Eintrag

ord-96d4e0fadccb4172846f3caba9247330

Quelldatensatz

uspto-grants-2013_07

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08497397B2