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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35328Generated: October 26, 2026

Potassium Iodide → 7-[4,4-bis(4-fluorophenyl)butyl]hexahydro-3,3-dimethylimidazo[1,5-a]pyrazin-1(5H)-one

https://huagongshe.com/reaction/35328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant1,1'-(4-Chlorobutylidene)bis(4-fluorobenzene)HCID 76820—
Reactanthexahydro-3,3-dimethylimidazo(1,5-a)pyrazin-1(5H)-oneHCID 14230278—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
Product7-[4,4-bis(4-fluorophenyl)butyl]hexahydro-3,3-dimethylimidazo[1,5-a]pyrazin-1(5H)-oneHCID 14230280—

Reaction Steps

A mixture of 169.8 parts of 1,1'-(4-chlorobutylidene)bis[4-fluorobenzene], 93.5 parts of hexahydro-3,3-dimethylimidazo[1,5-a]pyrazin-1(5H)-one, 128.3 parts of sodium carbonate, 0.1 parts of potassium iodide and 1200 parts of 4-methyl-2-pentanone was stirred and refluxed for 8 hours using a water-separator. After cooling overnight to room temperature, the reaction mixture was filtered. The filtrate was evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was triturated in 2,2'-oxybispropane. The product was filtered off and dried, yielding 108 parts of 7-[4,4-bis(4-fluorophenyl)butyl]hexahydro-3,3-dimethylimidazo[1,5-a]pyrazin-1(5H)-one; mp. 148.4° C. (intermediate 90).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766125
Source datasetuspto-grants-1988_08
ORD IDord-e6838801ccbd4ce59d0d38e7c8f17a03
Source noteuspto-grants-1988_08