Hydrazoic acid → HCID 178427292, compound
Reaction equation
[C:1]1([CH3:12])[CH:6]=[CH:5][C:4]([S:7]([C:10]#[N:11])(=[O:9])=[O:8])=[CH:3][CH:2]=1.[NH:13]=[N+:14]=[N-:15]>C1C=CC=CC=1>[C:1]1([CH3:12])[CH:2]=[CH:3][C:4]([S:7]([C:10]2[NH:15][N:14]=[N:13][N:11]=2)(=[O:8])=[O:9])=[CH:5][CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of p-toluenesulfonyl cyanide (0.0 g.) and excess hydrazoic acid in 50 ml. of benzene is stirred at room temperature for 20 hours. The product is filtered off, dissolved in ether, filtered through celite and evaporated to a solid which on trituration with benzene has a melting point, 133°-135° C.
Workup
- filtrationThe product is filtered off
- dissolutiondissolved in ether
- filtrationfiltered through celite
- customevaporated to a solid which on trituration with benzene
- customa melting point, 133°-135° C.
Sources & evidence
- ORD record
- ord-9131042ccf094d209fbcef9bf702c87c
- Source dataset
- uspto-grants-1985_07
- Patent number
- US04526978
Reaction notes
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