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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422890Generated: October 27, 2026

Hexane → 6-methoxy-2H-1-oxa-9-aza-phenanthrene-3-carbonitrile

https://huagongshe.com/reaction/1422890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantEthyl AcetateHCID 8857—
ReactantDabcoHCID 9237—
Reactant3-Hydroxy-6-methoxy-quinoline-4-carbaldehydeHCID 86671527—
SolventAcrylonitrileHCID 7855—
Product6-methoxy-2H-1-oxa-9-aza-phenanthrene-3-carbonitrileHCID 6724676478%

Reaction Steps

1,4-Diazabicyclo[2.2.2]octane (345 mg, 3.07 mmol, 0.25 eq) is added at room temperature to a stirred suspension of 3-hydroxy-6-methoxy-quinoline-4-carbaldehyde (2.5 g, 12.3 mmol, 1.0 eq) in acrylonitrile (25 mL) and the resulting mixture is heated under reflux for 60 hours. The reaction mixture is then cooled to room temperature and extracted with ethyl acetate (3×100 mL) and a 1N sodium hydroxide aqueous solution (50 mL). The combined organic layers are dried over sodium sulfate, filtered and concentrated to give a residue that is purified by column chromatography (silica gel, eluent: hexane:ethyl acetate, 5:1, v/v) to afford 6-methoxy-2H-1-oxa-9-aza-phenanthrene-3-carbonitrile as a light yellow solid (2.3 g, 78% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927541B2
Source datasetuspto-grants-2015_01
ORD IDord-7cad9b36509647fbb70874959c36184a
Source noteuspto-grants-2015_01