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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398497Generated: November 2, 2026

Hydrochloric Acid → 3-[4-(3-Diethylaminopropoxy)benzoyl]-2-phenylbenzothiophene

https://huagongshe.com/reaction/2398497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Phenylbenzo[b]thiopheneHCID 610886—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant4-(3-Diethylaminopropoxy)benzoyl chlorideHCID 21435261—
SolventCarbon DisulfideHCID 6348—
SolventCarbon disulfide methylene chlorideHCID 22764793—
Product3-[4-(3-Diethylaminopropoxy)benzoyl]-2-phenylbenzothiopheneHCID 21435257—

Reaction Steps

To a slurry of 4.0 g. (0.03 mol.) of anhydrous aluminum chloride in 30 ml. of carbon disulfide under a nitrogen atmosphere at 5° is added a mixture of 2.1 g. (0.01 mol.) of 2-phenylbenzothiophene in 40 ml. of 1:1 carbon disulfide-methylene chloride containing 3.06 g. (0.01 mol.) of 4-(3-diethylaminopropoxy)benzoyl chloride. After addition, the reaction mixture is warmed to ambient temperature and stirred for 16 hours. Dilute aqueous hydrochloric acid is added to the mixture and the layers are separated. The aqueous phase is re-extracted with chloroform and the organic layers are combined and concentrated to give a residue which is treated with ethereal hydrochloric acid and chromatographed on silica gel with methanol-chloroform as eluant to give the title compound as the corresponding hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04024273
Source datasetuspto-grants-1977_05
ORD IDord-fd10958e711d4730b5e902bf7d7bd1e1
Source noteuspto-grants-1977_05