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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082671Generated: October 31, 2026

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

https://huagongshe.com/reaction/1082671

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 (Na :SO,) 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 numberUS05589495
Source datasetuspto-grants-1996_12
ORD IDord-a4599c4ee8104409944c46cb4ec71214
Source noteuspto-grants-1996_12