HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 268396Generated: October 29, 2026
Hydrochloric Acid → 3-[4-(3-Diethylaminopropoxy)benzoyl]-2-phenylbenzothiophene
https://huagongshe.com/reaction/268396
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2-Phenyl-1-benzothiophene | HCID 610886 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 4-(3-Diethylaminopropoxy)benzoyl chloride | HCID 21435261 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Solvent | Carbon disulfide methylene chloride | HCID 22764793 | — |
| Product | 3-[4-(3-Diethylaminopropoxy)benzoyl]-2-phenylbenzothiophene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03947470 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-cbe5e8fbfd6648538389dce7d1173ec7 |
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| Source note | uspto-grants-1976_03 |
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