Hydrochloric Acid → 1-Cyclooctylmethylimidazole hydrochloride
Reaction equation
[CH:1]1([CH2:9][N:10]2[CH:14]=[CH:13][N:12]=[CH:11]2)[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[ClH:15]>CCOCC>[ClH:15].[CH:1]1([CH2:9][N:10]2[CH:14]=[CH:13][N:12]=[CH:11]2)[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1-Cyclooctylmethylimidazole (~0.3 g) was dissolved in dry ether (30 ml), when a stream of dry hydrogen chloride was passed through the solution at -20° C. The resulting white precipitate was filtered off under dry nitrogen and recrystallised from ethyl acetate/petroleum ether (b.p. 40°-60° C.) to afford 1-cyclooctylmethylimidazole hydrochloride as a white solid, m.p. 20°-22° C.
Workup
- customwas passed through the solution at -20° C
- filtrationThe resulting white precipitate was filtered off under dry nitrogen
- customrecrystallised from ethyl acetate/petroleum ether (b.p. 40°-60° C.)
Sources & evidence
- ORD record
- ord-5bdd3835cb974ba2bc4d7b9ee7b35fb0
- Source dataset
- uspto-grants-1982_03
- Patent number
- US04317830
Reaction notes
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