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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951977Generated: November 3, 2026

Hydrochloric Acid → HCID 19261375, compound

https://huagongshe.com/reaction/1951977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Bromo-4-hydroxybenzaldehydeHCID 76308—
CatalystCuprous chlorideHCID 62652—
Solvent1-ButanolHCID 263—
ProductHCID 19261375HCID 19261375161.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

4.3 g (188 mmol) of sodium is put at the bottom of a flask under nitrogen and 40 ml of 1-butanol is poured on top. The reaction mixture is stirred and heated progressively up to 120° C.; as the butanolate formed is sparingly soluble, 20 ml of 1-butanol is added. When all the sodium has been consumed, the reaction mixture is brought back to room temperature and 40 ml of dimethylformamide is added. Under nitrogen, 6.8 g (68.2 mmol) of copper(I) chloride is added and then 12.4 g (62 mmol) of 3-bromo-4-hydroxy-benzaldehyde. The reaction mixture is heated progressively to 120° C. and stirred for 2 hours. After cooling to room temperature and then acidifying to pH5 with aqueous hydrochloric acid of concentration 2M, the reaction mixture is extracted with ethyl acetate. The organic phases are combined, washed with saturated sodium chloride solution, dried over magnesium sulfate, filtered, and evaporated. After trituration and then recrystallization of the residue from pentane, 9.7 g (81%) of 3-butoxy-4-hydroxy-benzaldehyde is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404836B2
Source datasetuspto-grants-2013_03
ORD IDord-fb424e7dc84544c98e088d47ee6fc794
Source noteuspto-grants-2013_03