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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271265Generated: November 1, 2026

Acetic Acid → 5-(Benzyloxy)-2-(methoxycarbonyl)-1-tetralone

https://huagongshe.com/reaction/1271265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl CarbonateHCID 12021—
ReactantSodium hydrideHCID 24758—
Reactant5-(Benzyloxy)-1,2,3,4-tetrahydronaphthalen-1-oneHCID 10586915—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-(Benzyloxy)-2-(methoxycarbonyl)-1-tetraloneHCID 2293200198.2%

Reaction Conditions

Temperature82.5 °C

Reaction Steps

Under an argon atmosphere, 2.09 g of 60% sodium hydride was suspended in 30 ml of anhydrous dioxane and 11.51 g of dimethyl carbonate was added. While stirring with heating in an oil bath at 80 to 85° C., a solution of 6.58 g of 5-(benzyloxy)-1-tetralone in 15 ml of dioxane was added dropwise over about one hour. After stirring for one hour, the reaction solution was ice-cooled and 52 ml of an aqueous 1N acetic acid solution was added dropwise. The reaction solution was diluted with water, extracted with diethyl ether, washed with water 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 7.95 g of the desired compound as a pale yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205302B2
Source datasetuspto-grants-2007_04
ORD IDord-435f2a26a0204e24ab77c276ef29e0fd
Source noteuspto-grants-2007_04