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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088702Generated: October 26, 2026

Benzylamine → N-[6-[[6-(2-Pyridinyl)hexyl]oxy]hexyl]benzenemethanamine

https://huagongshe.com/reaction/1088702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant2-[6-[(6-Bromohexyl)oxy]hexyl]pyridineHCID 22161758—
ProductN-[6-[[6-(2-Pyridinyl)hexyl]oxy]hexyl]benzenemethanamineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963564
Source datasetuspto-grants-1990_10
ORD IDord-7943357c189e47a2a938a150b7705919
Source noteuspto-grants-1990_10