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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186882Generated: October 27, 2026

1-(4-Methoxyphenyl)butane-1,3-dione → 4-(4-Methoxybenzoyl)-5-methylisoxazole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1186882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Methoxyphenyl)butane-1,3-dioneHCID 77640—
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl chloro(hydroximino)acetateHCID 6816376—
SolventEthanolHCID 702—
Product4-(4-Methoxybenzoyl)-5-methylisoxazole-3-carboxylic acid ethyl esterHCID 59652027—

Reaction Steps

To 7.04 mL of 21% sodium ethoxide in ethanol (18.8 mmol) in 60 mL ethanol at 0° C. was added 4.70 g of 1-(4-methoxyphenyl)butane-1,3-dione (17.1 mmol) in 60 mL ethanol dropwise over 24 minutes. After 30 min a solution of 2.59 g of ethyl chloro-(hydroximino)acetate (17.1 mmol) in 30 mL ethanol was added dropwise over 6 minutes. The reaction was warmed to room temperature slowly. When TLC indicated the reaction was complete, the reaction was concentrated in vacuo. Water and saturated NaHCO3 was added and the product extracted with ethyl acetate. The ethyl acetate extracts were dried with Na2SO4, filtered, and concentrated in vacuo. The crude material was purified via silica gel chromatography eluting with 8:1 hexane:ethyl acetate to give 4-(4-methoxybenzoyl)-5-methylisoxazole-3-carboxylic acid ethyl ester which was dried overnight under high vacuum to give 3.74 g (71.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673916B2
Source datasetuspto-grants-2014_03
ORD IDord-4a4c50f72b504f5ba1d8e481940fc7e6
Source noteuspto-grants-2014_03