Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | N-Octylpyridin-4(1H)-imine | HCID 3017535 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 14198639 | HCID 14198639 | 83% |
Reaction Steps
A mixture of 4-octylaminopyridine (10 g., 0.048 mole) and octyl bromide (8 ml., 0.048 mole) was heated at 125° C. for 8 hr. on one day and for 4 more hr. on the next day. The resulting solid was slurried, first in ether, then in ether-tetrahydrofuran (2:1) and finally in tetrahydrofuran, collected by filtration, washed with ether on the filter, and dried (70° C., 0.1 mm.) affording N-(1-octyl-4(1H)-pyridinylidene)octanamine monohydrobromide (11.95 g., 83% yield, m.r. 108°-112° C.), which is the monohydrobromide salt of the compound of Formula I wherein both R and R' are octyl.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04839372 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-bce5a123b8344015b1b08e2a9a6dcbff |
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| Source note | uspto-grants-1989_06 |
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