HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → N-[6-[[6-(2-Pyridinyl)hexyl]oxy]hexyl]benzenemethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 2-[6-[(6-Bromohexyl)oxy]hexyl]pyridine | HCID 22161758 | — |
| Product | N-[6-[[6-(2-Pyridinyl)hexyl]oxy]hexyl]benzenemethanamine | HCID 22161746 | — |
Reaction Steps
2-[6-[(6-Bromohexyl)oxy]hexyl]pyridine (4.99 g) was added dropwise to benzylamine (22 ml) at 140° C. under nitrogen. The solution was stirred at 140° for 1 h and distilled under vacuum to remove benzylamine. The residue was partitioned between ethyl acetate (300 ml) and 8% aqueous sodium bicarbonate (200 ml). The dried organic layer was concentrated and the residual oil was purified by FCC eluting with ethyl acetate-triethylamine (100:1) to give the title compound as a pale yellow oil (4.65 g), t.l.c. (ethyl acetate+few drops triethylamine) Rf 0.23.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04963564 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-7943357c189e47a2a938a150b7705919 |
| Source note | uspto-grants-1990_10 |