Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271266Generated: November 3, 2026

Sodium borohydride → 5-(Benzyloxy)-1-hydroxy-2-(methoxycarbonyl)-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/1271266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-(Benzyloxy)-2-(methoxycarbonyl)-1-tetraloneHCID 22932001—
SolventMethanolHCID 887—
Product5-(Benzyloxy)-1-hydroxy-2-(methoxycarbonyl)-1,2,3,4-tetrahydronaphthaleneHCID 2293196274.5%

Reaction Steps

A solution of 7.95 g of 5-(benzyloxy)-2-(methoxycarbonyl)-1-tetralone in 80 ml of methanol was ice-cooled and 0.97 g of sodium borohydride was added in five portions. After stirring for 30 minutes, an ice bath was removed and the mixture was further stirred for 30 minutes. The reaction solution was diluted with iced water, extracted with diethyl ether, washed with water and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressured. The residue was purified by silica gel column chromatography to obtain 5.96 g of the desired compound as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205302B2
Source datasetuspto-grants-2007_04
ORD IDord-b8caffb593e74adbbac590c7ee342992
Source noteuspto-grants-2007_04