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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545315Generated: October 29, 2026

1,2-Dibromoethane → HCID 58198500, compound

https://huagongshe.com/reaction/545315

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 58198649HCID 58198649—
Catalyst18-Crown-6HCID 28557—
CatalystTetrabutylammonium BromideHCID 74236—
SolventAcetoneHCID 180—
ProductHCID 58198500HCID 58198500163%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a mixture of 1.69 g (5.69 mmol) of (4-trifluoromethyl-benzenesulfonyl) -acetic acid ethyl ester (prepared according step 1 and 2 of Method A), 1.59 g (11.5 mmol) of potassium carbonate, 100 mg 18-crown-6 and 100 mg tetrabutylammonium bromide in acetone (40 mL) were added 0.49 mL (5.69 mmol) of 1,2-dibromoethane. The reaction was heated in a sealed tube to 65° C. for 18 h. The mixture was filtered and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (silica, eluent heptanes, 0-20% ethyl acetate) to afford 2.99 g of 1-(4-trifluoromethyl -benzenesulfonyl)-cyclopropanecarboxylic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935715B2
Source datasetuspto-grants-2011_05
ORD IDord-0440cea5b09f43e0b618208f89fd8328
Source noteuspto-grants-2011_05