Butylamine → N-Butyl-3-methyl-1,2,4-oxadiazol-5-amine
Reaction equation
[CH3:1][C:2]1[N:6]=[C:5](C(Cl)(Cl)Cl)[O:4][N:3]=1.[CH2:11]([NH2:15])[CH2:12][CH2:13][CH3:14]>>[CH2:11]([NH:15][C:5]1[O:4][N:3]=[C:2]([CH3:1])[N:6]=1)[CH2:12][CH2:13][CH3:14]Participants
3
Procedure
3-Methyl-5-trichloromethyl-1,2,4-oxadiazole (43 g, 0.21 mole) was added to n-butylamine (46.75 g, 0.63 mole) and stirred at room temperature overnight. Excess amine was removed under vacuum and the residue distilled (oil bath 110° C./0.5 mm Hg). Recrystallisation fromm petroleum ether 60°-80° C. gave the title compound as white plates 26 g, m.p. 62°-65° C.
Workup
- customExcess amine was removed under vacuum
- distillationthe residue distilled (oil bath 110° C./0.5 mm Hg)
- customRecrystallisation fromm petroleum ether 60°-80° C.
Sources & evidence
- ORD record
- ord-1f11e51b8ea349ccade8b35962502bb4
- Source dataset
- uspto-grants-1979_07
- Patent number
- US04163048
Reaction notes
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