Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453879Generated: October 30, 2026

Iodine → HCID 68409296, compound

https://huagongshe.com/reaction/453879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantBromobenzeneHCID 7961—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
Reactant1-Benzyl-4-(dimethylamino)piperidine-4-carbonitrileHCID 16453915—
SolventDiethyl EtherHCID 3283—
SolventChloroform methanolHCID 21584188—
ProductHCID 68409296HCID 68409296160%

Reaction Conditions

Temperature80 °C

Reaction Steps

A little iodine was added to a mixture of 34.5 g (3.5 eq.) magnesium and 100 ml dry diethyl ether, followed over a period of 10 min by 10 g (0.15 eq.) bromobenzene, and the mixture was stirred for a further 10 min. Once the reaction had started, 183 g (2.85 eq.) bromobenzene dissolved in 500 ml diethyl ether were added dropwise over a period of 2 h and the mixture was stirred for a further 15 min. 100 g (1 eq.) 1-benzyl-4-(dimethylamino)piperidine-4-carbonitrile dissolved in 900 ml diethyl ether were added over a period of 2 h to the Grignard reagent prepared in the preceding step and the mixture was then heated for 12 h at 80° C. The reaction course was monitored by thin-layer chromatography (10% MeOH/CHCl3). Once the conversion was complete, the reaction solution was cooled to 0° C., mixed with saturated NH4Cl solution, extracted with ethyl acetate (3×300 ml) and the combined organic phases were dried with Na2SO4. Following removal of the solvent under reduced pressure, the residue was purified by column chromatography (silica gel; 1% MeOH/CHCl3). 30 g (35%) of product were obtained in the form of a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492559B2
Source datasetuspto-grants-2013_07
ORD IDord-d5b64f658ef94769bb957bba246a13e0
Source noteuspto-grants-2013_07