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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301895Generated: October 31, 2026

Hydrochloric Acid → 4-(5-Bromo-6-methoxy-2-naphthyl)-4-hydroxybut-3-en-2-one

https://huagongshe.com/reaction/2301895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantButyl AcetateHCID 31272—
Reactant1-(5-Bromo-6-methoxynaphthalen-2-yl)ethan-1-oneHCID 622178—
ReactantSodium MethoxideHCID 10942334—
SolventWaterHCID 962—
Product4-(5-Bromo-6-methoxy-2-naphthyl)-4-hydroxybut-3-en-2-oneHCID 70179405—

Reaction Conditions

Temperature65 °C

Reaction Steps

50 Grams (0.179 moles) of 2-acetyl-5-bromo-6-methoxynaphthalene and 200 ml of n-butyl acetate are placed in a flask equipped with refrigerator and stirrer and, under stirring and at the temperature of 15° C., 14.5 g (0.268 moles) of sodium methoxide are added. The temperature of the reaction mixture goes up to 25° C. and is kept at this value for 30 minutes, then the mixture is warmed at 65° C. for one hour, is added with 100 ml of water and is brought to pH 4 by adding a concentrated aqueous solution of hydrochloric acid. The reaction mixture is then cooled to 0°÷5° C. and kept at this temperature for one hour. The solid is filtered, abundantly washed with water on the filter, then washed with butyl acetate and dried in oven under vacuum obtaining 53 g of product with a yield equal to 92%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037813E1
Source datasetuspto-grants-2002_08
ORD IDord-c847674200be4e1bba461e7f93b851ad
Source noteuspto-grants-2002_08