Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251373Generated: November 1, 2026

1,2-Dibromoethane → Magnesium Bromide

https://huagongshe.com/reaction/1251373

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DibromoethaneHCID 7839—
ReactantFuranHCID 8029—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-PiperidinocyclohexanecarbonitrileHCID 62529—
ReactantMagnesium BromideHCID 82241—
ReactantMagnesiumHCID 5462224—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductMagnesium BromideHCID 82241—
ProductHCID 178418296HCID 178418296—

Reaction Steps

A solution of MgBr2 is prepared from 1,2-dibromo-ethane (6.76 g, 36 mmol, 4 eq) and magnesium (0.88 g, 36 mmol, 4 eq) in ether (80 ml) under a nitrogen atmosphere. A 2-lithio-furan solution is prepared under nitrogen atmosphere by adding a 1.6M solution of n-butyl-lithium in hexane (28 ml, 45 mmol, 5 eq) dropwise to a mixture of furan (3.1 g, 45 mmol, 5 eq) and TMEDA (5.2 g, 45 mmol, 5 eq) in anhydrous ether (100 ml) at −20° C. The mixture is then taken to reflux for 2 hours, cooled down to ambient temperature and MgBr2 in ether is added dropwise to the solution. A 1-piperidin-1-yl-cyclohexanecarbonitrile (1.7 g, 9 mmol, 1 eq) solution in ether is added dropwise at ambient temperature. The mixture is taken to reflux for 16 hours, cooled down to ambient temperature, then treated in the following manner: the mixture is poured gently into an ice-cooled saturated solution of NH4Cl, agitated for 30 minutes, extracted with ether; the ethereal phases are combined, then extracted three times with 10% HCl, and 20% NH4OH is added to the aqueous phase until neutrality. The aqueous phase is extracted with ether, the organic phase is washed with water, dried over Na2SO4, filtered and concentrated under vacuum. The crude product is purified by chromatography on alumina with CH2Cl2 as eluent in order to produce an oil (1.7 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342511B1
Source datasetuspto-grants-2002_01
ORD IDord-c3e238acc68d44b4923c678d58532a7f
Source noteuspto-grants-2002_01