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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495024Generated: October 25, 2026

Catechol → 4-Fluoro-2H-1,3-benzodioxole

https://huagongshe.com/reaction/495024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCatecholHCID 289—
ReactantDibromomethaneHCID 3024—
Reactant3-FluorocatecholHCID 67764—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
Product4-Fluoro-2H-1,3-benzodioxoleHCID 15767260—

Reaction Steps

Alliquat 336 (methyltrioctylammonium chloride (0.63 g, 0.0016 mol), 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, 6.1 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 1.5 hours. The resulting dark mixture was heated an additional 2 hours at reflux. After cooling to room temperature, the reaction was diluted with methylene chloride and water. The aqueous layer was extracted with methylene chloride and the combined organic layers were dried and concentrated to give 1-fluoro-2,3-methylenedioxybenzene (14.6 g, 104.2 mmol) as a dark yellow oil: 1H NMR (CDCl3): δ 6.80 (m, 1H), 6.68 (m, 2H), 6.04 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538214B2
Source datasetuspto-grants-2009_05
ORD IDord-3eb7de94d4b447aca1624806392c413c
Source noteuspto-grants-2009_05