Reaction #1355157

ord-c6b436b8ce7945a68973626ef1926cec

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherHCl (g) bubbled into the solution until saturated
  2. 2
    Concentrationconcentrated in vacuo

Procedure

A solution of (2R)-3-benzyloxy-2-(N-(t-butoxycarbonyl)amino)propanoic acid (23 g, 78 mmol, [α]D−4.4°(c=2, H2O)) in methanol (250 mL) was cooled to 0° C. and HCl (g) bubbled into the solution until saturated. The resulting mixture was stirred at ambient temperature for 17 hours and then concentrated in vacuo to afford 17 g (100% yield) of (2R)-3-benzyloxy-2-aminopropanoic acid methyl ester, a compound of formula (M), as a white solid; NMR (DMSO-d6) 8.7 (br s, 3), 7.4-7.3 (m, 5), 4.5 (q, 2), 4.4 (br s, 1), 3.8 (s, 2), 3.7 (s, 3) ppm.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06555537B2uspto-grants-2003_04