Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488145Generated: October 28, 2026

Hydrochloric Acid → HCID 14986479, compound

https://huagongshe.com/reaction/488145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 14986468HCID 14986468—
SolventEthanolHCID 702—
ProductHCID 14986479HCID 1498647947.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

0.5 g of ethyl (E)-3-(4-acetoxy-3-isopropyl-5-methyl-1-naphthyl)propenoate was dissolved in 50 ml of ethanol, to which a potassium hydroxide aqueous solution (potassium hydroxide 1.6 g/water 10 ml) was added, followed by refluxing for 30 minutes. The solution was cooled to 0° C. and water was added. Dilute hydrochloric acid was added to make the aqueous phase acidic and extracted with ethyl acetate. The organic phase was washed with brine, dried with anhydrous magnesium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography (40% ethyl acetate/hexane) and the resultant crystals were recrystallized from a mixed solvent of isopropyl ether and ethyl acetate (1:1) and washed with isopropyl ether and hexane (3:7) to obtain 0.19 g of the titled compound as yellow needle.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298649
Source datasetuspto-grants-1994_03
ORD IDord-7a19aefef5c74ad18e8c67d5e387bc49
Source noteuspto-grants-1994_03