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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887048Generated: October 26, 2026

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

https://huagongshe.com/reaction/887048

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 numberUS08247414B2
Source datasetuspto-grants-2012_08
ORD IDord-8f43d294955747ae9d8d9980fb7b361b
Source noteuspto-grants-2012_08