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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421582Generated: November 2, 2026

Bromine → 1,2-Dibromo-4,5-diethoxy-3-fluorobenzene

https://huagongshe.com/reaction/2421582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium AcetateHCID 517045—
Reactant5-Bromo-1,2-diethoxy-3-fluorobenzeneHCID 59668392—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product1,2-Dibromo-4,5-diethoxy-3-fluorobenzeneHCID 11709889101.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 5-bromo-1,2-diethoxy-3-fluorobenzene (40.0 g, 0.15 mol) in acetic acid (200 mL), sodium acetate (16.2 g, 0.20 mol) and bromine (31.6 g, 0.20 mol) were added sequentially at room temperature, and the mixture was stirred at 50° C. for 1.5 hours. The reaction mixture was cooled to room temperature, and a saturated aqueous solution of sodium thiosulfate (400 mL) and water (400 mL) were added sequentially. The mixture was extracted once with heptane (800 mL) and three times with heptane (400 mL). The organic layer was washed sequentially with water (400 mL), once with a 2 N aqueous solution of sodium hydroxide (200 mL), once with a 2 N aqueous solution of sodium hydroxide (100 mL), and water (400 mL), then dried over anhydrous magnesium sulfate. The solvent was distilled off from the organic layer under reduced pressure and the residue was filtered. The filtrate was then purified by silica gel column chromatography (hexane, ethyl acetate) to give 52.0 g of the title compound (yield:quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956222B2
Source datasetuspto-grants-2011_06
ORD IDord-7633cd7d9e024e218a460e833c48e025
Source noteuspto-grants-2011_06