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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295944Generated: October 30, 2026

1,2-Dibromoethane → 1-[4-(2-Bromoethoxy)-3-(tert-butyl)-5-nitrophenyl]-1-ethanone

https://huagongshe.com/reaction/1295944

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant1-[3-(Tert-butyl)-4-hydroxy-5-nitrophenyl]-1-ethanoneHCID 22929728—
SolventDimethylformamideHCID 6228—
Product1-[4-(2-Bromoethoxy)-3-(tert-butyl)-5-nitrophenyl]-1-ethanoneHCID 2292967069.8%

Reaction Steps

Potassium carbonate (4.65 g, 33.7 mmol) and 1,2-dibromoethane (31.7 g, 166.6 mmol) were added to a solution of 1-[3-(tert-butyl)-4-hydroxy-5-nitrophenyl]-1-ethanone (8.0 g, 33.7 mmol) in dimethylformamide (200 ml) and the mixture was stirred at room temperature for 12 hours. Ethyl acetate was added, the reaction mixture was washed with water and brine in that order and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield 1-[4-(2-bromoethoxy)-3-(tert-butyl)-5-nitrophenyl]-1-ethanone (8.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244730B2
Source datasetuspto-grants-2007_07
ORD IDord-61e43feaafaa413aa50c4c690d6ee472
Source noteuspto-grants-2007_07