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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271268Generated: November 3, 2026

Sodium Hydroxide → 5-(Benzyloxy)-2-(hydroxymethyl)-3,4-dihydronaphthalene

https://huagongshe.com/reaction/1271268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant5-(Benzyloxy)-2-(methoxycarbonyl)-3,4-dihydronaphthaleneHCID 22932012—
SolventDichloromethaneHCID 6344—
SolventDiisobutylaluminumhydrideHCID 21225700—
Product5-(Benzyloxy)-2-(hydroxymethyl)-3,4-dihydronaphthaleneHCID 2293202189.1%

Reaction Steps

Under an argon atmosphere, to a solution of 2.79 g of 5-(benzyloxy)-2-(methoxycarbonyl)-3,4-dihydronaphthalene in 30 ml of dry dichloromethane, 24 ml of diisobutylaluminum hydride (1M toluene solution) was added dropwise at −70° C. or lower, followed by stirring for 20 minutes. To the reaction solution, 26 ml of an aqueous 10% sodium hydroxide solution was added dropwise and, after heating to room temperature, the mixture was extracted with diethyl ether. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to obtain 2.25 g of the desired compound as a colorless crystal having a melting point of 59 to 61° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205302B2
Source datasetuspto-grants-2007_04
ORD IDord-058514802e3b4bd8aa1af909efe752e8
Source noteuspto-grants-2007_04