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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2240670Generated: November 1, 2026

2-Bromo-1-(2,4-dichlorophenyl)ethan-1-one → HCID 68585005, compound

https://huagongshe.com/reaction/2240670

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(2,4-dichlorophenyl)ethan-1-oneHCID 75828—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66755815HCID 66755815—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 68585005HCID 6858500570%

Reaction Conditions

Temperature35 °C

Reaction Steps

To a solution of 5-(3-amino-phenyl)-1,1-dioxo-[1,2,5]thiadiazolidin-3-one (5 g, 22 mmol) in 37.5 mL of 9:1 v/v acetonitrile-water was added NaHCO3 (4.62 g, 55 mmol). The mixture was stirred at 25° C. while 2-bromo-1-(2,4-dichloro-phenyl)-ethanone (7.1 g, 26.4 mmol) was added. The mixture was stirred for 12-16 hours at 35° C. The mixture was cooled on an ice bath to further precipitate the product, which was then collected by filtration. The filtrate was concentrated under reduced pressure and a second crop of crude product was collected. The combined crude product washed once with 25 mL water and dried, then washed once with 10 mL methyl tert-butyl ether and dried, to provide 6.36 g (70% yield) of 5-{3-[2-(2,4-dichloro-phenyl)-2-oxo-ethylamino]-phenyl}-1,1-dioxo-[1,2,5]thiadiazolidin-3-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723369B2
Source datasetuspto-grants-2010_05
ORD IDord-f31b4750963b42c5b16d42f0435accb5
Source noteuspto-grants-2010_05