Acetone → Ethyl 2,2-difluoro-3-(isopropylamino)propanoate

Temperatur

0 °C

Ethyl 3-(dibenzylamino)-2,2-difluoropropanoate (5.00 g, 15.0 mmol) was dissolved in EtOH (25 mL) and trifluoroacetic acid was added (1.15 mL, 15.5 mmol). To this mixture, Pd(OH)2/C (20%, 250 mg) was added, and the reaction mixture was hydrogenated at 60 psi overnight. The mixture was filtered through a pad of Celite, the Celite pad was washed with ethanol and the filtrate was concentrated in vacuo. The residue was dissolved in THF (65 mL) and to the solution was added acetone (0.872 g, 15.0 mmol) and sodium acetate (1.23 g, 15.0 mmol). The reaction mixture was cooled to 0° C. and NaBH(OAc)3 (4.77 g, 22.5 mmol) was added in portions over 5 min. The mixture was stirred vigorously at room temperature overnight and then was poured into a cold (0° C.) brine solution (100 mL). The pH was adjusted to 12.5 with NaOH (50%) and the mixture was extracted with ethyl acetate (3×50 mL). The combined organic extract were dried (MgSO4) and concentrated in vacuo to afford the title compound as a clear light yellow oil (1.54 g, 54%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.04 (d, J=6.32 Hz, 6 H) 1.36 (t, J=7.20 Hz, 3 H) 2.73-2.94 (m, 1 H) 3.20 (t, J=13.52 Hz, 2 H) 4.34 (q, J=7.24 Hz, 2 H)

1. customwas hydrogenated at 60 psi overnight
2. filtrationThe mixture was filtered through a pad of Celite
3. washthe Celite pad was washed with ethanol
4. concentrationthe filtrate was concentrated in vacuo
5. dissolutionThe residue was dissolved in THF (65 mL) and to the solution
6. extractionthe mixture was extracted with ethyl acetate (3×50 mL)
7. extractionThe combined organic extract
8. dry with materialwere dried (MgSO4)
9. concentrationconcentrated in vacuo

ORD-Eintrag

ord-e3ce4e03162e45658872ac85faee005a

Quelldatensatz

uspto-grants-2012_11

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08318727B2