Formanilide → Phenyl isocyanate
Reaction equation
[C:1]1([NH:7][CH:8]=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>C(#N)C1C=CC=CC=1>[C:1]1([N:7]=[C:8]=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The experiment of Example X was repeated in such a way that a mixture of phenyl formamide and benzonitrile was evaporated at a rate of 5 ml/hour in a gas stream of 110 liters of nitrogen and 3 liters of air/hour. The gas mixture also comprised carbon disulphide, which was fed at a rate of 0.67% per hour, calculated on the added amount by weight of n-hexyl formamide. Use of the same catalyst bed as in Example XIX at a temperature of 375° C. resulted in a yield of phenyl isocyanate of 41% at a selectivity of 74%.
Workup
- customwas evaporated at a rate of 5 ml/hour in a gas stream of 110 liters of nitrogen and 3 liters of air/hour
Sources & evidence
- ORD record
- ord-54d17eef3a5b425bbf984b4f7d466ed3
- Source dataset
- uspto-grants-1980_06
- Patent number
- US04207251
Reaction notes
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