Reaction #1688908

ord-3108fa6b6e3b4dc9a3e03c6ca4aa6a6c

Solvents

Conditions

Temperature
50°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Concentrationhydrolyzed at 0° C. with 100 ml of 3N hydrochloric acid, subsequently concentrated to a volume of 125 ml
  2. 2
    workup.ADDITIONdiluted with 125 ml of water
  3. 3
    Temperaturecooled to 0° C.
  4. 4
    Filtrationfiltered
  5. 5
    WashThe residue was washed with water/isopropanol (4:1)
  6. 6
    Otherdried

Procedure

25.57 g of methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)-carbamate were added portionwise at 22° C. to a suspension of 21.44 g of aluminum isopropoxide in 260 ml of isopropanol. The suspension was stirred at 50° C./400 mbar for 2 hours, hydrolyzed at 0° C. with 100 ml of 3N hydrochloric acid, subsequently concentrated to a volume of 125 ml, diluted with 125 ml of water, cooled to 0° C. and filtered. The residue was washed with water/isopropanol (4:1) and dried, there being obtained 13.01 g (89%) of isomerically-pure methyl (1S,2S)-(1-benzyl-3-chloro 2-hydroxy-propyl)-carbamate, m.p. 162°-163.5° C. IR (KBr): 3323s, br. (NH, OH), 1689 (C=O), 1546s (amide II).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05977388uspto-grants-1999_11