Sec-Butylamine → HCID 23335972, compound
Reaction equation
[Cl:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[C:6](Cl)[C:5]([N+:12]([O-:14])=[O:13])=[CH:4][C:3]=1[CH3:15].[CH:16]([NH2:20])([CH2:18][CH3:19])[CH3:17]>C1CCCCC1>[CH:16]([NH:20][C:6]1[C:5]([N+:12]([O-:14])=[O:13])=[CH:4][C:3]([CH3:15])=[C:2]([Cl:1])[C:7]=1[N+:8]([O-:10])=[O:9])([CH2:18][CH3:19])[CH3:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 10.04 g. (0.04 mole) of 2,4-dichloro-3,5-dinitrotoluene, 5.85 g. (0.08 mole) of sec-butylamine and 200 ml. of cyclohexane is stirred at reflux for six hours. The mixture is filtered and the filtrate is evaporated at reduced pressure. The filtrate is partitioned between ether and dilute hydrochloric acid. The organic phase is washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. Crystallization of the residue from ethanol gives 7.71 g. of orange crystals, m.p. 40°-46° C. Two recrystallizations from ethanol give the analytical sample, m.p. 45°-47° C. Analysis Calcd. for C11H14ClN3O4 : C, 45.92; H, 4.90; Cl, 12.32; N, 14.61. Found: C, 45.96; H, 4.97; Cl, 12.36; N, 14.78.
Workup
- additionA mixture of 10.04 g
- temperatureat reflux for six hours
- filtrationThe mixture is filtered
- customthe filtrate is evaporated at reduced pressure
- customThe filtrate is partitioned between ether and dilute hydrochloric acid
- washThe organic phase is washed with water and brine
- dry with materialdried over magnesium sulfate
- customevaporated in vacuo
- customCrystallization of the residue from ethanol
- customgives 7.71 g
- customTwo recrystallizations from ethanol
- customgive the analytical sample, m.p. 45°-47° C
Sources & evidence
- ORD record
- ord-17f6df8d810e4ec594a8d4e68bb45deb
- Source dataset
- uspto-grants-1980_10
- Patent number
- US04227913
Reaction notes
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