HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854025Generated: October 26, 2026
Water → 6-(4-Bromobenzyl)oxy-2-(N,N-dimethylamino)methyltetralin
https://huagongshe.com/reaction/854025
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | 2-(N,N-Dimethylamino)methyl-6-hydroxytetralin | HCID 21939764 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(4-Bromobenzyl)oxy-2-(N,N-dimethylamino)methyltetralin | HCID 18361535 | 37.3% |
Reaction Steps
2-(N,N-Dimethylamino)methyl-6-hydroxytetralin (5.0 g; obtained in Reference Example 16) was dissolved in DMF (130 ml), to which was added 60% oily sodium hydride (1.46 g) at 0° C. The reaction mixture was warmed to room temperature, and stirred for 1 hour. This was again cooled to 0° C., to which was added a DMF solution (20 ml) of 4-bromobenzyl bromide (10.0 g). The reaction mixture was stirred at room temperature for 2 hours, and water was added thereto, 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:ethyl acetate/hexane=1/10) to obtain the entitled compound (3.4 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-50e0bc4335c04ad38feeaae7af4432df |
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| Source note | uspto-grants-2007_08 |
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