Nitric Acid → HCID 20286805, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[CH:6]=[CH:5][C:4]=1[S:11]([OH:14])(=[O:13])=[O:12].C(Cl)(Cl)Cl.[N+:19]([O-])([OH:21])=[O:20]>C(#N)C>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[C:6]([N+:19]([O-:21])=[O:20])=[CH:5][C:4]=1[S:11]([OH:14])(=[O:13])=[O:12]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution prepared by adding 90 g of 2,4-dimethoxybenzenesulfonic acid obtained in Step (1) above to 200 ml of chloroform, was added 225 ml of nitric acid (d=1.42) with stirring. The reaction mixture was stirred at 25° to 30° C. for 2 hours and 300 ml of acetonitrile was added thereto. The crystals thus-precipitated were collected by filtration and washed with 100 ml of acetonitrile.
Workup
- customTo a solution prepared
- stirringThe reaction mixture was stirred at 25° to 30° C. for 2 hours
- customThe crystals thus-precipitated
- filtrationwere collected by filtration
- washwashed with 100 ml of acetonitrile
Sources & evidence
- ORD record
- ord-44fd202d4bf3468394e8bd57ea9730ac
- Source dataset
- uspto-grants-1981_03
- Patent number
- US04255509
Reaction notes
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