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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881771Generated: October 30, 2026

1,4-Dibromobenzene → HCID 86700876, compound

https://huagongshe.com/reaction/881771

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobenzeneHCID 7804—
Reactant4-MethylenecyclohexanoneHCID 573489—
ReactantMagnesiumHCID 5462224—
CatalystIodineHCID 807—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86700876HCID 8670087636.7%

Reaction Steps

To a flask charged with dry, freshly ground magnesium turnings (1.1 g, 45 mmol) and iodine (25 mg, 0.1 mmol) in THF (50 mL) was added a solution of 1,4-dibromobenzene (10.6 g, 45.0 mmol) in THF (30 mL) slowly by dropping funnel over 30 min. The resulting mixture was stirred at rt for 1 hr. The resultant grey Grignard solution was cooled to −78° C. and to it was added a solution of 4-methylenecyclohexanone (3.3 g, 30 mmol) in THF (20 mL) slowly dropwise over 20 min. The reaction was stirred at −78° C. for 30 min before being allowed to stir and warm to rt for 3 h. The resulting reaction mixture was quenched with a saturated aqueous NH4Cl solution and extracted with methyl tert-butyl ether. The combined organic phases were washed with a saturated aqueous NaCl solution, dried over MgSO4, filtered and concentrated by rotary evaporation in vacuo to afford a crude yellow oil. Purification of the crude material by column chromatography (80 g silica gel, 0-50% EtOAc:Hept, monitor for 225 nm) afforded 2.94 g of a colorless oil that was used without further purification. ESI-MS m/z: not ionized [M+H]+, retention time 1.50 min (condition E).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993619B2
Source datasetuspto-grants-2015_03
ORD IDord-e1d785dcd0bf4346bfd4f741ec5d4dce
Source noteuspto-grants-2015_03