Propyl isocyanate → HCID 15550543, compound
Reaction equation
[C:1]([C:5]1[CH:6]=[C:7]([CH:10]=[C:11]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:12]=1[OH:13])[CH:8]=[O:9])([CH3:4])([CH3:3])[CH3:2].[CH2:18]([N:21]=[C:22]=[O:23])[CH2:19][CH3:20]>CN(C=O)C>[CH2:18]([NH:21][C:22]([O:13][C:12]1[C:5]([C:1]([CH3:4])([CH3:3])[CH3:2])=[CH:6][C:7]([CH:8]=[O:9])=[CH:10][C:11]=1[C:14]([CH3:17])([CH3:16])[CH3:15])=[O:23])[CH2:19][CH3:20]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared in DMF using 3,5-di-tert-butyl-4-hydroxybenzaldehyde and n-propyl isocyanate according to the procedure described in Example H. The title compound was isolated in 100.0% yield as an off-white solid.
Sources & evidence
- ORD record
- ord-92870d53e8eb471f89c35846d48449f3
- Source dataset
- uspto-grants-2006_02
- Patent number
- US06998419B2
Reaction notes
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