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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387946Generated: October 31, 2026

Iodine → HCID 68408396, compound

https://huagongshe.com/reaction/2387946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantButyl bromideHCID 8002—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
Reactant1-Benzyl-4-(dimethylamino)piperidine-4-carbonitrileHCID 16453915—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventChloroform methanolHCID 21584188—
ProductHCID 68408396HCID 6840839653.8%

Reaction Steps

To a mixture of 17.7 g (6 equiv.) of magnesium and 50 ml of dry ether there were added first a small amount of iodine and then, over a period of 1 hour, 100 g (6 equiv.) of bromobutane dissolved in 100 ml of dry ether. This reaction mixture was stirred for 1 hour at room temperature. The Grignard reagent prepared above was added over a period of 20 minutes to a solution of 30 g (1 equiv.) of 1-benzyl-4-(dimethylamino)piperidine-4-carbonitrile dissolved in 210 ml of dry THF, and the resulting reaction mixture was then stirred for 12 hours at room temperature. The progress of the reaction was monitored by thin-layer chromatography (10% MeOH/CHCl3). When the reaction was complete, the reaction solution was cooled to 0° C.; saturated NH4Cl solution was added, the mixture was filtered over Celite and extracted with ethyl acetate (3×200 ml), and the combined organic phases were dried over Na2SO4. After removal of the solvent under reduced pressure, purification was carried out by column chromatography (aluminium oxide neutral; hexane). 18.2 g (53%) of product were obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08269000B2
Source datasetuspto-grants-2012_09
ORD IDord-074fc0482100479382204fb4c16d4a0c
Source noteuspto-grants-2012_09