Butyl isocyanate → HCID 54048187, compound
Reaction equation
[OH:1][N:2]1[C:7]([CH3:9])([CH3:8])[CH2:6][CH:5]([NH2:10])[CH2:4][C:3]1([CH3:12])[CH3:11].[CH2:13]([N:17]=[C:18]=[O:19])[CH2:14][CH2:15][CH3:16]>C1(C)C=CC=CC=1>[CH2:13]([NH:17][C:18]([NH:10][CH:5]1[CH2:6][C:7]([CH3:8])([CH3:9])[N:2]([OH:1])[C:3]([CH3:12])([CH3:11])[CH2:4]1)=[O:19])[CH2:14][CH2:15][CH3:16]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of 1.0 g of 1-oxyl-4-amino-2,2,6,6-tetramethylpiperidine in 75 mL of dry toluene is added dropwise 0.65 mL of butyl isocyanate. The reaction mixture is stirred for 16 hours. The solution is then concentrated to yield the title compound as a red oil.
Workup
- concentrationThe solution is then concentrated
Sources & evidence
- ORD record
- ord-39c3d63dc36b41bda9d049fa45e330f1
- Source dataset
- uspto-grants-1999_07
- Patent number
- US05928558
Reaction notes
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