Acetic Acid → 2-Oxazolidinone, 4-phenyl-, (4S)-

Temperature

0 °C

To a stirred, 0° C. solution of L-phenylglycine (25.3 g, 167.4 mmol) in 60 mL of 3N aqueous NaOH was added ethyl chloroformate (8 mL) in several portions. Additional 3N aqueous NaOH (35 mL) was added to redissolve the precipitated phenylglycine, followed by ethyl chloroformate (4 mL). This process was continued with 3N aqueous NaOH (65 mL) and ethyl chloroformate (8 mL, total of 20 mL, 209 mmol) over a period of ca. 10 minutes. After stirring for 1 hour at 0° C. the solution was acidified with 6 M H2SO4, and the precipitated carbamate was extracted into 8% isopropanol in dichloromethane (2×300 mL). The combined organic layers were dried (Na2SO4) and concentrated to afford 37.3 g of N-ethoxycarbonyl L-phenylglycine as a white solid. The carbamate was dissolved in 170 mL of THF, cooled to 0° C., treated with borane-dimethylsulfide (33.5 mL of a 10 M solution), and stirred at room temperature for 17 hours. Excess borane was cautiously quenched with water (100 mL), and the bulk of the THF removed under reduced pressure. The white slurry was diluted with additional water (350 mL) and then extracted with dichloromethane (2×500 mL). The combined organic layers were washed with 100 mL of saturated aqueous NaHCO3, dried (Na2SO4), and concentrated to give 27.4 g of (S)-2-ethoxycarbonylamino-2-phenylethanol as a white solid. The crude alcohol was dissolved in 200 mL of THF, cooled to 0° C., and treated with n-butyllithium in hexane (6 mL of a 2 M solution). After heating at 55° C. for 6 hours, the solution was treated with acetic acid (1 ml) and concentrated. The residue was dissolved in dichloromethane (300 mL), washed with 100 mL of brine, dried (Na2SO4), and concentrated to a white solid. Recrystallization from toluene gave 17.14 g (63%) of (S)-4-phenyloxazolidin-2-one; mp 132°-133° C.; [α]D20 +49.5° (c=2.1, CHCl3); IR (CHCl3) 3460, 3020, 1760, 1500, 1480, 1460, 1400, 1230 cm-1 ; 1HNMR δ7.45-7.30 (m, 5, ArH), 6.42 (br s, 1, NH), 4.96 (br t, 1, J=7.8 Hz, OCH2CH), 4.72 (t, 1, J=8.6 Hz, one of OCH2CH), 4.17 (dd, 1, J=6.7, 8.7 Hz; one of OCH2CH).

1. temperatureAfter heating at 55° C. for 6 hours
2. concentrationconcentrated
3. dissolutionThe residue was dissolved in dichloromethane (300 mL)
4. washwashed with 100 mL of brine
5. dry with materialdried (Na2SO4)
6. concentrationconcentrated to a white solid
7. customRecrystallization from toluene

ORD record

ord-2ad1856091174d6092d488a46dc59680

Source dataset

uspto-grants-1988_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04775752