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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510340Generated: October 26, 2026

1,2-Dibromoethane → tert-Butyl 1-acetylcyclopropanecarboxylate

https://huagongshe.com/reaction/1510340

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantPotassium CarbonateHCID 11430—
ReactantTert-butyl acetoacetateHCID 15538—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 1-acetylcyclopropanecarboxylateHCID 5743436556,111.102%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of tert-butyl acetoacetate (497 mL, 3.00 mol), 1,2-dibromoethane (310 mL, 3.60 mmol), potassium carbonate (1.106 k g, 8.00 mmol), and dimethylformamide (2.0 L) was stirred in a water bath at 30° C. for 1.5 hours, in a water bath at 60° C. for 3.5 hours, and in a water bath at 30° C. for 4 days. The reaction mixture was separated by filtration through celite, and the residue on the celite was washed with diethylether (3.5 L). The filtrate and the diethylether used for the washing were combined and added to water (2 L), and the organic layer was separated. The aqueous layer was extracted with diethylether (2 L), and water (1 L) was added to the resulting aqueous layer, and further extraction was conducted by adding diethylether (2 L). All organic layers were combined, and washed with 10% aqueous solution of citric acid (2 L), water (2 L×3), and saturated aqueous solution of sodium chloride (2 L×3), and dried by adding anhydrous sodium sulfate. After removing the dessicating agent by filtration, the solvent was removed by distillation under reduced pressure, and the residue was distilled under reduced pressure to obtain 371.8 g of the target compound (10 mmHg, distillation fraction of 72 to 78° C., 2.02 mol, 67%) as a colorless transparent oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211910B2
Source datasetuspto-grants-2012_07
ORD IDord-7bd01e9b11eb472b8afa90e871a4536e
Source noteuspto-grants-2012_07