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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18684Generated: October 25, 2026

Hydrochloric Acid → 2-Butyl-3-(4-iodobenzyl)-1,3-diazaspiro[4.4]non-1-en-4-one

https://huagongshe.com/reaction/18684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Iodobenzyl bromideHCID 954258—
Reactant2-Butyl-1,3-diazaspiro[4.4]non-1-en-4-oneHCID 10176511—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-Butyl-3-(4-iodobenzyl)-1,3-diazaspiro[4.4]non-1-en-4-oneHCID 1199642688%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 23.07 g (100 mmol) of the hydrochloride of 2-butyl-1,3-diazaspiro[4,4]non-1-en-4-one and 19.8 g of potassium hydroxide in 100 mL de water is added to a solution of 29.7 g (100 mmol) of 4-iodobenzyl bromide and 3.4 g (10 mmol) of tetrabutylammonium bisulphate in 30 mL of toluene, and the mixture is heated at reflux for 1 hr. After cooling to 25° C., 100 mL of water is added and the phases are separated. To the organic phase is added 10 mL of concentrated hydrochloric acid, 100 mL is evaporated at reduced pressure, 300 mL of ethyl acetate is added and the resulting solid is filtered to give 39.6 g (88%) of the title compound in the form of hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741492B2
Source datasetuspto-grants-2010_06
ORD IDord-cfa93898b13c4cddbdf0bab68e95b661
Source noteuspto-grants-2010_06