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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534684Generated: November 4, 2026

Ethyl bromoacetate → HCID 53700452, compound

https://huagongshe.com/reaction/1534684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantHCID 54231235HCID 54231235—
SolventDimethylformamideHCID 6228—
ProductHCID 53700452HCID 5370045253.9%

Reaction Steps

To a suspension of 310 mg of 60% oily sodium hydride in 10 ml of dry DMF was added dropwise a solution of 2.8 g of 2-n-heptyl-2'-hydroxy-4'-(3-methyl-2-butenyloxy)chalcone in 10 ml of DMF with ice cooling. Then, 1.2 g of ethyl bromoacetate was added, and the mixture was stirred at room temperature for an hour. After neutralization with dilute hydrochloric acid, 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 chromatographed on silica gel column with n-hexane containing 1% ethyl acetate to give 1.83 g of 2'-ethoxycarbonylmethoxy-2-n-heptyl-4'-(3-methyl-2-butenyloxy)-chalcone. To a solution of this compound in 30 ml of ethanol was added 15 ml of 10% aqueous potassium carbonate solution, and the mixture was stirred at 60° C. for 4.5 hours. After neutralization with dilute hydrochloric acid with ice cooling, the precipitated solid was collected by filtration and recrystallized from ethanol to give 1.23 g of 2'-carboxymethoxy-2-n-heptyl-4'-(3-methyl-2-butenyloxy)chalcone as pale yellow plates.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089654
Source datasetuspto-grants-1992_02
ORD IDord-6d63aa86a77149b683f7a0eb60010c61
Source noteuspto-grants-1992_02