HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854038Generated: October 26, 2026
Sodium Chloride → 2-(N,N-Dimethylamino)methyl-6-(4'-methoxybiphenyl-4-yl)methoxytetralin hydrochloride
https://huagongshe.com/reaction/854038
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Methoxyphenyl boric acid | HCID 14769994 | — |
| Reactant | 6-(4-Bromobenzyl)oxy-2-(N,N-dimethylamino)methyltetralin | HCID 18361535 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(N,N-Dimethylamino)methyl-6-(4'-methoxybiphenyl-4-yl)methoxytetralin hydrochloride | HCID 18361570 | — |
Reaction Steps
6-(4-Bromobenzyl)oxy-2-(N,N-dimethylamino)methyltetralin (374 mg; obtained in Reference Example 33) and tetrakis-(triphenylphosphine) palladium (35 mg) were dissolved in toluene (8 ml), to which were added an ethanol solution (1 ml) of 4-methoxyphenylboric acid (198 mg) and an aqueous 2 M sodium carbonate solution (1 ml). The reaction mixture was heated under reflux for 6 hours in an argon atmosphere. A saturated aqueous sodium chloride solution was added to this, which was then extracted with ethyl acetate. The organic layer was dried, and then concentrated. The residue was purified by alumina column chromatography (eluent:ethyl acetate/hexane=1/10), and then processed with 4 N hydrochloric acid-ethyl acetate to form a hydrochloride. The thus-formed salt was recrystallized from ethanol-ethyl acetate to obtain the entitled compound (0.290 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07256204B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-346db62f956d4d689d99ddf11fcbc829 |
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| Source note | uspto-grants-2007_08 |
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