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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054446Generated: November 1, 2026

Hydrogen Bromide → 5-Bromo-7-fluoro-2,3-dihydrobenzo[b][1,4]dioxine

https://huagongshe.com/reaction/1054446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium NitriteHCID 23668193—
Reactant7-Fluoro-2,3-dihydro-1,4-benzodioxin-5-amineHCID 66680600—
SolventWaterHCID 962—
Product5-Bromo-7-fluoro-2,3-dihydrobenzo[b][1,4]dioxineHCID 89635954—

Reaction Steps

NaNO2 (2.69 g, 39.9 mmol) in water (20 mL) was added slowly at 0° C. to a solution of 7-fluoro-2,3-dihydrobenzo[b][1,4]dioxin-5-amine (4.5 g, 26 mmol) in aq. 47% HBr (20 mL) and continued stirring at same temperature for 30 min. The above diazonium salt solution was added slowly to a solution of CuBr (5.7 g, 39.9 mmol) in aq. 47% HBr (25 mL) at 0° C. and stirred at 25° C. for 30 min. Reaction mixture was quenched with ice water, extracted with ethyl acetate (3×50 mL), washed it with water followed by brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure to afford crude. The crude was purified by column purification (using silica gel and 0-5% ethyl acetate in Hexane as eluent) to afford 5-bromo-7-fluoro-2,3-dihydrobenzo[b][1,4]dioxine (Int-28) (5.9 g). 1H NMR (300 MHz, CDCl3) δ 6.9-6.84 (1H, dd), 6.6-6.5 (1H, dd), 4.3-4.3 (4H, m) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394305B2
Source datasetuspto-grants-2016_07
ORD IDord-cdfa4b24b41041958c6c4102f335dc2f
Source noteuspto-grants-2016_07