反应详情

To a stirred solution of 3-fluoro-3-(4-formyl-phenyl)-azetidine-1-carboxylic acid tert-butyl ester (4.5 g, 16.11 mmol, 1 eq) in mixture of methanol (50 mL) and water (40 mL) was added hydroxyl amine hydrochloride (1.66 g, 24.17 mmol, 1.5 eq) followed by addition of sodium acetate (2.37 g, 29.0 mmol, 1.8 eq) at room temperature. Resulting reaction mixture was stirred at room temperature for 24 hours. After complete consumption of starting material, reaction mixture was concentrated in vacuo to afford to yellow colored residue, which was diluted by water (120 mL) and extracted with ethyl acetate (3×80 mL). Combined organic phase was washed with brine solution (70 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure to get yellow semi solid (2.3 g, Crude). Crude was purified by Combiflash using 40 g Redisep column. Desired compound was eluted in 19% ethyl acetate in hexane to afford title compound as yellow semi solid (1.0 g, 21.1%). 1H NMR (400 MHz, CDCl3) δ: 1.47 (s, 9H), 4.20-4.27 (m, 2H), 4.36-4.44 (m, 2H), 7.47 (d, J=8.28 Hz, 2H), 7.64 (d, J=8.2 Hz, 2H), 8.13 (s, 1H). LC-MS (m/z): 293.1 (M−H).

1. customResulting
2. customreaction mixture
3. customAfter complete consumption of starting material, reaction mixture
4. concentrationwas concentrated in vacuo
5. customto afford to yellow colored residue, which
6. extractionextracted with ethyl acetate (3×80 mL)
7. washCombined organic phase was washed with brine solution (70 mL)
8. dry with materialdried over anhydrous Na2SO4
9. concentrationconcentrated under reduced pressure
10. customto get yellow semi solid (2.3 g, Crude)
11. customCrude was purified by Combiflash
12. washDesired compound was eluted in 19% ethyl acetate in hexane