Reaction equation
[CH2:1]([NH:5][C:6]1[O:7][CH:8]=[C:9]([CH3:11])[N:10]=1)[CH2:2][CH2:3][CH3:4].[CH2:12]([N:15]=[C:16]=[O:17])[CH:13]=[CH2:14]>C1C=CC=CC=1>[CH2:12]([NH:15][C:16]([N:5]([CH2:1][CH2:2][CH2:3][CH3:4])[C:6]1[O:7][CH:8]=[C:9]([CH3:11])[N:10]=1)=[O:17])[CH:13]=[CH2:14]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2-butylamino-4-methyloxazole (12.0 g, 0.078 mol) and allyl isocyanate (6.46 g, 0.078 mol) in dry benzene was heated under reflux for 4 hours, and worked up as described in Example 3. The product was further purified by chromatography on a silica-gel column, eluting with a 1:1 mixture of benzene and ethyl acetate.
Workup
- temperatureunder reflux for 4 hours
- customThe product was further purified by chromatography on a silica-gel column
- washeluting with a 1:1 mixture of benzene and ethyl acetate
Sources & evidence
- ORD record
- ord-13bc78d337a34709a28e20131cf08c96
- Source dataset
- uspto-grants-1979_11
- Patent number
- US04175131
Linked notes
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