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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751555Generated: October 30, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → 5-fluoro-8-methoxy-2H-chromene

https://huagongshe.com/reaction/751555

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant6-Fluoro-2-hydroxy-3-methoxybenzaldehydeHCID 22482818—
ReactantHCID 178477248HCID 178477248—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product5-fluoro-8-methoxy-2H-chromeneHCID 2248284535.1%

Reaction Steps

6-Fluoro-2-hydroxy-3-methoxy-benzaldehyde (3.32 g, 19 mmol) was dissolved in acetonitrile (20 ml) and DBU (2.97 ml, 19 mmol) was added followed by vinyltriphenylphosphine bromide (7.2 g, 19 mmol). The reaction mixture was heated under reflux for 48 h, diluted with water and extracted with ether (3×50 ml). The organic phase was washed with water, 10% sodium hydroxide, water and brine and evaporated in vacuo. The residue was submitted to column chromatography (silica gel, EA:Hex, 1:20) yielding 1.2 g of 5-fluoro-8-methoxy-2H-chromene (34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405310B2
Source datasetuspto-grants-2008_07
ORD IDord-1c9dc8d7bfb84757baf8de51ec6d1e22
Source noteuspto-grants-2008_07