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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392658Generated: October 26, 2026

Hydrochloric Acid → 3,4-Dioctylthiophene

https://huagongshe.com/reaction/392658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3,4-DibromothiopheneHCID 18452—
ReactantHCID 178443577HCID 178443577—
CatalystHCID 178418745HCID 178418745—
SolventDiethyl EtherHCID 3283—
Product3,4-DioctylthiopheneHCID 2194561682.9%

Reaction Steps

2 M octylmagnesium bromide (100 milliliters, 0.2 mol) in anhydrous ethyl ether was added to a well-stirred mixture of dichloro[1,3-bis(diphenylphosphino)-propane]nickel(II) (0.2 gram) and 3,4-dibromothiophene (20.16 grams, 0.0833 mol) in 200 milliliters of anhydrous ethyl ether in a 500 milliliter round bottom flask cooled with an ice bath under an inert atmosphere. The nickel complex reacted immediately with the Grignard reagent and the resulting reaction mixture was allowed to warm up to room temperature. An exothermic reaction started within 30 minutes and the ethyl ether began to reflux gently. After stirring for another 2 hours at room temperature, the reaction mixture was refluxed for 6 hours, then cooled in an ice bath, and hydrolyzed with aqueous 2N hydrochloric acid. The organic layer was separated and washed successively with water, brine, and again with water, dried over anhydrous sodium sulfate, and filtered. After evaporation of the solvent, the residue was distilled under reduced pressure through Kugelrohr apparatus to provide 21.3 grams of 3,4-dioctylthiophene as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06803262B2
Source datasetuspto-grants-2004_10
ORD IDord-c216d78066b7406f9caa978d72799d47
Source noteuspto-grants-2004_10