HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166535Generated: October 26, 2026
Dimethylformamide → 6-(4-Biphenylyl)methoxy-2-[3-(N,N-dimethylamino)propyl]tetralin hydrochloride
https://huagongshe.com/reaction/1166535
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Phenylbenzyl chloride | HCID 15463 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-[3-(N,N-dimethylamino)propyl]-6-hydroxytetralin | HCID 18361546 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(4-Biphenylyl)methoxy-2-[3-(N,N-dimethylamino)propyl]tetralin hydrochloride | HCID 18361597 | — |
Reaction Steps
60% Oily sodium hydride (0.258 g) was added to a DMF solution (20 ml) of 2-[3-(N,N-dimethylamino) propyl]-6- hydroxytetralin (1.00 g) at 0° C. The reaction mixture was warmed to room temperature, and stirred for 30 minutes. This was again cooled to 0° C., and 4-(chloromethyl)biphenyl (1.04 g) as added thereto, and then stirred at room temperature for 4 hours. Water was added to the reaction mixture, which was then extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution, then dried, and concentrated. The residue was purified by alumina column chromatography (eluent: toluene alone to toluene/ethyl acetate=1/1), and then processed with 4 N hydrochloric acid-ethyl acetate to form a hydrochloride. The thus-formed salt was recrystallized from methanol-diisopropyl ether to obtain the entitled compound (1.30 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06613805B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-522be3fdb85d4e848a2bb0d01fcc1856 |
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| Source note | uspto-grants-2003_09 |
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