Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456471Generated: October 30, 2026

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

https://huagongshe.com/reaction/1456471

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-(1,3dithian-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 numberUS05843949
Source datasetuspto-grants-1998_12
ORD IDord-17876a2370184e4c956f75f38b1d0443
Source noteuspto-grants-1998_12