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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182029Generated: October 31, 2026

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

https://huagongshe.com/reaction/2182029

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 numberUS06894177B2
Source datasetuspto-grants-2005_05
ORD IDord-7b07348a7ed74736bd82b8ff697e2b41
Source noteuspto-grants-2005_05