3-Methoxybenzaldehyde → 5-[(3-Methoxyphenyl)methylene]-3-methyl-2,4-imidazolidinedione
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[CH:6]=O.[CH3:11][N:12]1[C:16](=[O:17])[CH2:15][NH:14][C:13]1=[O:18]>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:6]=[C:15]2[NH:14][C:13](=[O:18])[N:12]([CH3:11])[C:16]2=[O:17])[CH:8]=[CH:9][CH:10]=1Participants
3
Procedure
Prepared according to the procedure described in Example 93 using 3-methoxybenzaldehyde (3.5 ml, 28 mmoles) and 3-methyl hydantoin (3.0 g, 21 mmoles), to afford the product (3.6 g), mp 203°-205° C.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-abc10b3117c4434c8d090edccda1cf9d
- Source dataset
- uspto-grants-1994_04
- Patent number
- US05306822
Reaction notes
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