Acetic Anhydride → 4-Oxazolecarboxylic acid, 2-(acetylamino)-, ethyl ester
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[N:7]=[C:8]([NH2:11])[O:9][CH:10]=1)=[O:5])[CH3:2].[C:12](OC(=O)C)(=[O:14])[CH3:13]>>[CH2:1]([O:3][C:4]([C:6]1[N:7]=[C:8]([NH:11][C:12](=[O:14])[CH3:13])[O:9][CH:10]=1)=[O:5])[CH3:2]Participants
3
Procedure
1.0 g (6.40 mmol) 2-Amino-oxazole-4-carboxylic acid ethyl ester and 9.1 mL (96.3 mmol) acetic acid anhydride are stirred for 2 d at rt. The mixture is concentrated in vacuo to yield the desired product which is used without further purification.
Workup
- concentrationThe mixture is concentrated in vacuo
Sources & evidence
- ORD record
- ord-57cff594de224c42a16d335ca7ca622e
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08530461B2
Reaction notes
Loading…