Beta-Alanine → N-acryloyl-beta-alanine
Reaction equation
[C:1](Cl)(=[O:4])[CH:2]=[CH2:3].[NH2:6][CH2:7][CH2:8][C:9]([OH:11])=[O:10]>>[C:1]([NH:6][CH2:7][CH2:8][C:9]([OH:11])=[O:10])(=[O:4])[CH:2]=[CH2:3]Participants
3
Procedure
This amide monomer was prepared from acryloyl chloride and beta-alanine per Example 1 procedure, with the recrystallized (ethyl acetate solvent) product having a melting point of 97°-99° C.
Workup
- customwith the recrystallized (ethyl acetate solvent) product
Sources & evidence
- ORD record
- ord-bfebe56fe65c40d686ce3aad063559be
- Source dataset
- uspto-grants-1994_11
- Patent number
- US05369142
Reaction notes
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