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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249375Generated: November 1, 2026

Catechol → 4-Fluorobenzo[d][1,3]dioxole

https://huagongshe.com/reaction/2249375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCatecholHCID 289—
ReactantWaterHCID 962—
ReactantDibromomethaneHCID 3024—
Reactant3-FluorocatecholHCID 67764—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
Product4-Fluorobenzo[d][1,3]dioxoleHCID 15767260—

Reaction Steps

Alliquat 336 (methyltrioctylammonium chloride, 0.63 g, 1.6 mmol), dibromomethane (40.7 g, 234.2 mmol) and water (31 mL) were placed in a 500 mL 3-necked flask equipped with an addition funnel, condenser and a stir bar. The addition funnel was charged with a solution of 3-fluorocatechol (20.0 g, 160 mmol) in 5M sodium hydroxide (80 mL). The mixture in the flask was heated to reflux and the solution of the catechol was added dropwise with good stirring over 2 hours and the resulting dark mixture heated an additional 2 hours at reflux. After cooling to room temperature, the reaction was diluted with methylene chloride and the layers separated. The aqueous layer was extracted with methylene chloride and the combined organic layers dried (Na2SO4 with charcoal). Filtration and concentration to a constant weight on the rota-vap gave 1-fluoro-2,3-methylenedioxybenzene (14.6 g, 104.2 mmol) as a dark yellow oil: 1H NMR (CDCl3); 6.80 (m, 1H), 6.68 (m, 2H), 6.04 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314849B2
Source datasetuspto-grants-2008_01
ORD IDord-04314cbb4c7b43d4aaafbf6f282a03e9
Source noteuspto-grants-2008_01