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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72602Generated: October 26, 2026

Oxalyl chloride → (2-Bromo-5-iodo-phenyl)-chroman-6-yl-methanone

https://huagongshe.com/reaction/72602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantChromanHCID 136319—
Reactant2-Bromo-5-iodobenzoic acidHCID 2735572—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(2-Bromo-5-iodo-phenyl)-chroman-6-yl-methanoneHCID 5834080188.5%

Reaction Steps

To a stirred solution of 2-bromo-5-iodobenzoic acid (1.0 g, 3.06 mmol) in DCM (5 mL) was added DMF (0.2 mL) and oxalyl chloride (0.44 mL, 4.59 mmol) at 0° C. After complete addition, the reaction mixture was stirred at room temperature for 3 h. The volatiles were evaporated under reduced pressure, and the crude product was dissolved in DCM (4 mL) and added to chroman (488 mg, 3.67 mmol) which had been cooled to 0° C. To this mixture was added aluminum chloride (488 mg, 3.67 mmol) in portions. After stirring for 4 h, the reaction was quenched by pouring it into crushed ice. This was extracted with dichloromethane (50 mL×2). The dichloromethane layers were combined and washed with water (20 mL), saturated aqueous sodium bicarbonate solution (20 mL×2), and brine (20 mL), then dried over sodium sulfate, and concentrated. The crude product was purified by column chromatography to furnish (2-bromo-5-iodo-phenyl)-chroman-6-yl-methanone (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828951B2
Source datasetuspto-grants-2014_09
ORD IDord-8ab0cf2821234239adecb0e80d871d50
Source noteuspto-grants-2014_09