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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847297Generated: November 2, 2026

Methyl Ethyl Ketone → HCID 15106525, compound

https://huagongshe.com/reaction/847297

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 numberUS05140046
Source datasetuspto-grants-1992_08
ORD IDord-4e571c5231e54cb882556d81423aa4b6
Source noteuspto-grants-1992_08