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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534683Generated: November 3, 2026

Sodium Hydroxide → HCID 54231235, compound

https://huagongshe.com/reaction/1534683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2'-Hydroxy-4'-(3-methyl-2-butenyloxy)acetophenoneHCID 10932968—
ReactantHCID 18417656HCID 18417656—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 54231235HCID 5423123552.2%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 3.11 g of 2-heptylbenzaldehyde and 3.35 g of 2'-hydroxy-4'-(3-methyl-2-butenyloxy)-acetophenone in 65 ml of isopropanol was added a solution of 2.9 g of sodium hydroxide in 6 ml of water under a nitrogen atmosphere, and the mixture was stirred at 45° C. for 8 hours. After neutralization with dilute hydrochloric acid with ice cooling, the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography with n-hexane including 1% ethyl acetate. The resulting fractions containing the end compound was recrystallized from isopropanol to give 3.23 g of 2-n-heptyl-2'-hydroxy-4'-(3-methyl-2-butenyloxy)-chalcone as yellow needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089654
Source datasetuspto-grants-1992_02
ORD IDord-14c7f836cf2a448d944851c28c111bac
Source noteuspto-grants-1992_02