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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223253Generated: October 29, 2026

Potassium Carbonate → 6-Chloro-3{1-[4,4-bis(4-fluorophenyl)-1-butyl]-4-piperidyl}-1,2-benzisoxazole hydrochloride

https://huagongshe.com/reaction/223253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,1'-(4-Chlorobutylidene)bis(4-fluorobenzene)HCID 76820—
Reactant6-Chloro-3-(piperidin-4-yl)benzo[d]isoxazoleHCID 13076430—
SolventDimethylformamideHCID 6228—
Product6-Chloro-3{1-[4,4-bis(4-fluorophenyl)-1-butyl]-4-piperidyl}-1,2-benzisoxazole hydrochlorideHCID 1307837562.7%

Reaction Steps

A mixture of 16.5 g of 6-chloro-3-(4-piperidyl)-1,2-benzisoxazole, 22.4 g of 4-chloro-1,1-bis(4-fluorophenyl)butane, 22.0 g of potassium carbonate and 200 ml of dimethylformamide was stirred and heated at 75° for 5 hrs. The reaction mixture was allowed to cool and was filtered. The filtrate was concentrated in vacuo to an oil, which was taken up in 300 ml ether and washed with an equal portion of brine. The ether layer was dried over anhydrous sodium sulfate and concentrated in vacuo to an oil. The oil was dissolved in 65 ml of ethanol, the solution was cooled, and 20 ml of ether saturated with hydrogen chloride was added dropwise. Ether (400 ml) was added causing turbidity. The mixture was seeded and then stirred for 1/2 hour to produce the salt. Recrystallization from 800 l of 3:5 ethanol-ether gave 11.3 g (13% yield) of product, mp 205°-207°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04352811
Source datasetuspto-grants-1982_10
ORD IDord-ecb64508315143698f68b0fd0fdbad8c
Source noteuspto-grants-1982_10