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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266993Generated: October 25, 2026

1,4-Dibromobutane → 4-(4-Bromobutyl)-1-(1,3-dithian-2-yl)ethylbenzene

https://huagongshe.com/reaction/266993

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantEthyl AcetateHCID 8857—
Reactant4-Bromo-1-(1,3-dithian-2-yl)ethylbenzeneHCID 21960112—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Bromobutyl)-1-(1,3-dithian-2-yl)ethylbenzeneHCID 21960129—

Reaction Steps

A solution of 4-bromo-1-(1,3-dithian-2-yl)ethylbenzene (27.2 g, 94 mmol) in tetrahydrofuran (200 ml) was charged with sec-butyllithium (99 ml, 1.3M in cyclohexane, 0.13 mole) dropwise at -78° C. under nitrogen. The mixture was stirred at ambient temperature for 1.5 hours, and then quenched with 1,4-dibromobutane (42 g, 0.2 mole). After being stirred for 3 hours, the mixture was poured into ethyl acetate, and then washed with water and brine. The organic solution was then dried (Na2SO4) and concentrated to an oil. The crude product was purified by flash chromatography over a silica gel column. The 4-(4-bromobutyl)-1-(1,3-dithian-2-yl)-ethylbenzene thus purified was a light oil, 22.3 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652241
Source datasetuspto-grants-1997_07
ORD IDord-ed8fba15c4a645598a0f337106839cd0
Source noteuspto-grants-1997_07