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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967729Generated: October 30, 2026

Triethylamine → 8-Methoxy-6H-11-oxa-6-aza-benzo[a]fluoren-5-one

https://huagongshe.com/reaction/967729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Hydroxy-5-methoxybenzonitrileHCID 7022529—
Reactantalpha-BromodimethylhomophthalateHCID 131725194—
SolventAcetonitrileHCID 6342—
SolventSodium BicarbonateHCID 516892—
Product8-Methoxy-6H-11-oxa-6-aza-benzo[a]fluoren-5-oneHCID 11637529—

Reaction Steps

α-Bromodimethylhomophthalate (20a) (1.16 g) and 2-hydroxy-5-methoxy-benzonitrile (0.6 g, 4 mmol, 1 eq) were dissolved by warming in acetonitrile (6 mL). Triethylamine (5.6 mL, 10 eq) was then added and the reaction was heated at reflux for 48 h under inert atmosphere, then cooled to room temperature. The reaction mixture was diluted with saturated sodium bicarbonate (40 mL) and the resulting suspension was allowed to stir for 2 h, and was then filtered. The filtercake was washed sequentially with 1 N HCl (2×50 mL), acetonitrile (2×50 mL) and dichloromethane (50 mL), then dried in a vacuum oven at 50° C. for three days to provide Compound 22a as an white solid. Yield=0.81 g (76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06956035B2
Source datasetuspto-grants-2005_10
ORD IDord-0784b5b5b0464a1b9470530301fef300
Source noteuspto-grants-2005_10