Reaction #487579

ord-848cedc94b4846c4936411ac200eaa1c

Reaction equation

C=CC(=O)OCC
ethyl acrylate
CCOC(=O)CN.Cl
ethyl glycinate hydrochloride
[Na+].[OH-]
sodium hydroxide
CCOC(=O)CCNCC(=O)OCC
Diethyl-2-azabutane-1,4-dicarboxylate

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherAfter 19 h the solution was partitioned with dichloromethane (3×100 mL)
  2. 2
    DryingThe organic layer was dried with anhydrous sodium sulfate
  3. 3
    Filtrationfiltered
  4. 4
    Otherevaporated
  5. 5
    workup.DISTILLATIONThe residue was distilled
  6. 6
    Otherto afford AA (28.8 g, 61%)

Procedure

A 4.7 M aqueous solution of sodium hydroxide (50 mL) was added into a stirred, ice-cooled solution of ethyl glycinate hydrochloride (32.19 g, 0.23 mole) in water (50 mL). Then, ethyl acrylate (23.1 g, 0.23 mole) was added and the mixture was stirred at room temperature until completion of the reaction was ascertained by TLC. After 19 h the solution was partitioned with dichloromethane (3×100 mL). The organic layer was dried with anhydrous sodium sulfate, filtered and evaporated. The residue was distilled to afford AA (28.8 g, 61%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08741866B2uspto-grants-2014_06