Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982235Generated: October 30, 2026

Methyl Ethyl Ketone → HCID 15106525, compound

https://huagongshe.com/reaction/982235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantEthyl bromoacetateHCID 7748—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 15106507HCID 15106507—
CatalystTetrabutylammonium BromideHCID 74236—
ProductHCID 15106525HCID 15106525—

Reaction Conditions

Temperature60 °C

Reaction Steps

A catalytic amount of tetra-n-butylammonium bromide was added to a mixture of 0.64 g of 4-hydroxy-2-[p-(4-phenylbutoxy)benzamido]phenoxyacetic acid obtained in Example 78, 0.50 g of anhydrous potassium carbonate, 0.60 g of ethyl bromoacetate and 8 ml of 2-butanone followed by stirring at 60° C. for 4 hours. The reaction mixture was diluted with ethyl acetate and insoluble materials were filtered off. After the filtrate was washed with water and dried over anhydrous magnesium sulfate, the solvent was distilled off. The obtained solid was recrystallized from ethanol to obtain 0.83 g of ethyl [[4-ethoxycarbonylmethoxy-2-[p-(4-phenylbutoxy)benzamido]phenoxy]acetoxy]acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04994479
Source datasetuspto-grants-1991_02
ORD IDord-f88cc726298c485981d309ee54ba38db
Source noteuspto-grants-1991_02