Hydrochloric Acid → (3S)-3-([(1,1-dimethylethyl)oxy]carbonylamino)-2-hydroxy-4-phenylbutyl ethanoate

Temperature

-20 °C

To a suitable reactor was added the crude 3a in EtOH solution (about 153 mL) reserved from the previous step at 20-30° C. under N2. The mixture was cooled to −25 to −15° C., and NaBH4 (2.35 g) in water (60 mL) was added at below −8° C. The reaction mixture was warmed to −5-5° C. and stirred for 1 hr. The reaction was deemed completed as determined by TLC. 1N HCl aqueous solution (60 mL) was added at below 10° C. The mixture was warmed to 20-30° C., and H2O (183 mL) was added at this temperature. After being stirred at 20-30° C. for 1 hr, the mixture was further cooled to 0-5° C. and stirred for 1 hr. The mixture was filtered, and the filtered cake was washed with cold 50% EtOH aqueous solution (30 mL). The combined filtrate and washing was concentrated at 40-50° C. under reduced pressure to afford crude 4a as a white powder (18.7 g).

1. customreserved from the previous step at 20-30° C. under N2
2. temperatureThe reaction mixture was warmed to −5-5° C.
3. temperatureThe mixture was warmed to 20-30° C.
4. stirringAfter being stirred at 20-30° C. for 1 hr
5. temperaturethe mixture was further cooled to 0-5° C.
6. stirringstirred for 1 hr
7. filtrationThe mixture was filtered
8. washthe filtered cake was washed with cold 50% EtOH aqueous solution (30 mL)
9. washThe combined filtrate and washing
10. concentrationwas concentrated at 40-50° C. under reduced pressure

ORD record

ord-42eca575c6844a6a99b1f47231b6d2e4

Source dataset

uspto-grants-2014_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08722921B2