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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382953Generated: October 25, 2026

Water → 6-(4-Bromobenzyl)oxy-2-(N,N-dimethylamino)methyltetralin

https://huagongshe.com/reaction/382953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromobenzyl bromideHCID 68527—
Reactant2-(N,N-Dimethylamino)methyl-6-hydroxytetralinHCID 21939764—
SolventDimethylformamideHCID 6228—
Product6-(4-Bromobenzyl)oxy-2-(N,N-dimethylamino)methyltetralinHCID 1836153537.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310107B1
Source datasetuspto-grants-2001_10
ORD IDord-6e98dee0e6814b37ac858bc46a771f6a
Source noteuspto-grants-2001_10