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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458804Generated: October 29, 2026

Bromoacetyl bromide → HCID 18442580, compound

https://huagongshe.com/reaction/458804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantHCID 18442568HCID 18442568—
SolventDichloromethaneHCID 6344—
ProductHCID 18442580HCID 1844258070.1%

Reaction Conditions

Temperature-5 °C

Reaction Steps

1-(2-Amino-4,5-dimethoxy-phenyl)-2-(3,4-dichloro-phenyl)-ethanone (5.52 g, 16.24 mmol) was dissolved in dichloromethane (20 ml), distilled water was then added (2 ml) and the resulting solution was cooled at −5° C. under nitrogen. Bromoacetylbromide (1.63 ml, 18.68 mmol) was dissolved in dichloromethane (10 ml) and added dropwise to the previous solution; the temperature was not allowed to exceed +5° C. The reaction mixture was stirred at 0° C. for 15 min and then allowed to reach the RT before further stirring for 2.5 h. Dichloromethane was added (30 ml) and the organic layer was washed with distilled water, saturated NaHCO3 solution, and brine. It was dried over magnesium sulfate, filtered and the solvent was removed under vacuum. This crude mixture was purified by flash chromatography (dichloromethane/methanol, 360/1) to give the product as a yellow solid (5.25 g, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192950B2
Source datasetuspto-grants-2007_03
ORD IDord-5da54e4f22054c43afc4f3c7f4c9049b
Source noteuspto-grants-2007_03