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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107819Generated: October 31, 2026

18-Crown-6 → HCID 54041294, compound

https://huagongshe.com/reaction/1107819

Reaction equation

Participants

RoleNameHCIDCharge
Reactant18-Crown-6HCID 28557—
Reactant2-Butene, 1-bromo-HCID 122414—
ReactantHCID 18785698HCID 18785698—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54041294HCID 5404129453%

Reaction Steps

0.82 g (0.00731 mole) of potassium tert-butoxide was added to a solution of 1.39 g (0.00567 mole) of 5-[3-(4-fluorophenyl)propionyl]-2,3-dimethylpyrrole and 0.19 g (0.00074 mole) of 18-crown-6 in 40 ml of tetrahydrofuran and the resulting mixture was stirred at room temperature for 20 minutes. 1.80 g (0.0115 mole) of 1-bromo-2-butene (a mixture of cis and trans isomers) were added to the mixture and stirred at room temperature for 4 hours. After completion of the reaction, the reaction mixture was poured into ice-water and the aqueous mixture was extracted twice with 80 ml each of ethyl acetate. The extract was wahed with a saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the residue was purified by column chromatography through silica gel using a 1:10 mixture of ethyl acetate and hexane as an eluent to give 0.90 g of the title compound (cis/trans=22/78) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063782
Source datasetuspto-grants-2000_05
ORD IDord-3a74f07fb7814adb86d3037774e8a266
Source noteuspto-grants-2000_05