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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161671Generated: October 29, 2026

1,3-Benzodioxole → 1-Bromo-3,4-(methylenedioxy)benzene

https://huagongshe.com/reaction/1161671

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-BenzodioxoleHCID 9229—
ReactantLithium BromideHCID 82050—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1-Bromo-3,4-(methylenedioxy)benzeneHCID 75831—

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of ceric ammonium nitrate (9.88 g, 18.0 mmol) and lithium bromide (1.5 g, 18.0 mmol) in acetonitrile (20 mL) was stirred for 30 minutes at 25° C. under nitrogen atmosphere. A solution of benzo[1,3]dioxol (2 g, 16 mmol) in acetonitrile (20 mL) was added slowly to it and the mixture was stirred for 4 hours at 25° C. The mixture was then diluted with water (50 mL) and extracted with ethyl acetate (3×50 mL). The organic layers were collected, combined, washed with water (50 mL), dried over anhydrous sodium sulphate, and concentrated under vacuum to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820654B2
Source datasetuspto-grants-2010_10
ORD IDord-1a28b934bcd84d12bac9f20b610b4af7
Source noteuspto-grants-2010_10