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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118344Generated: November 2, 2026

6-Bromohexylbut-3-ynyl ether → 1-{4-[(6-Bromohexyl)oxy]-1-butyn-1-yl}-3-(cyclopentylsulfonyl)benzene

https://huagongshe.com/reaction/2118344

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromohexylbut-3-ynyl etherHCID 11379281—
Reactant1-(Cyclopentylsulfonyl)-3-iodobenzeneHCID 69119714—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
Product1-{4-[(6-Bromohexyl)oxy]-1-butyn-1-yl}-3-(cyclopentylsulfonyl)benzeneHCID 69119823—

Reaction Steps

A solution of 4-[(6-bromohexyl)oxy]-1-butyne (DE 3513885 A1) (288.9 mg) and 1-(cyclopentylsulfonyl)-3-iodobenzene (500 mg) in MeCN (20 ml) and triethylamine (345 μl) was treated with copper iodide (11.78 mg) and dichlorobis(triphenylphosphine)palladium(II) (43.4 mg) and stirred at room temperature for 3 h. The reaction mixture was partitioned between EtOAc and water, the organic phase was dried (MgSO4) and concentrated in vacuo. The mixture was purified by column chromatography (SPE bond elut, gradient 0 to 40% diethyl ether in cyclohexane) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442839B2
Source datasetuspto-grants-2008_10
ORD IDord-2c07afdb60d3435aba64de0bcabd2747
Source noteuspto-grants-2008_10