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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72608Generated: October 25, 2026

1,4-Benzodioxan → Methanone, (2-bromo-5-iodophenyl)(2,3-dihydro-1,4-benzodioxin-6-yl)-

https://huagongshe.com/reaction/72608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-BenzodioxanHCID 10301—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-Bromo-5-iodobenzoyl chlorideHCID 58340809—
SolventDichloromethaneHCID 6344—
ProductMethanone, (2-bromo-5-iodophenyl)(2,3-dihydro-1,4-benzodioxin-6-yl)-HCID 5834079888.4%

Reaction Steps

To a stirred solution of 2-bromo-5-iodo-benzoyl chloride (26.4 g, 76.56 mmol) in dichloromethane (250 mL) was added benzo(1,4)-dioxane (10.41 g, 76.26 mmol) at 0° C. To this reaction mixture, AlCl3 (40.78 g, 305.47 mmol) was added in portions. After stirring overnight at room temperature, the reaction mixture was poured into crushed ice. The resulting mixture was extracted with dichloromethane (500 mL×2). The dichloromethane layers were combined and washed with water (200 mL), saturated aqueous sodium bicarbonate solution (200 mL×2), and brine (200 mL), then dried over sodium sulfate and concentrated. The solid product was triturated with hexanes, and the triturated product was dried under vacuum to furnish (2-bromo-5-iodo-phenyl)-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-methanone (30 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828951B2
Source datasetuspto-grants-2014_09
ORD IDord-c8555ad84cbe4978bc56d977b4700fb0
Source noteuspto-grants-2014_09