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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647553Generated: October 28, 2026

Methanol → Ethyl 3-methyl-2-(2-oxoethyl)butanoate

https://huagongshe.com/reaction/647553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 13246109HCID 13246109—
ProductEthyl 3-methyl-2-(2-oxoethyl)butanoateHCID 1324611089%

Reaction Steps

In 100 g of methanol were dissolved 10.0 g of ethyl α-allylisovalerate (general formula [XI] wherein R=--CH2CH3) and, under cooling at -20°~-10° C. and stirring, ozone gas was bubbled into the solution for 8 hours. Then, at room temperature, the reaction mixture was added to 100 g of dimethyl sulfide and the mixture was stirred at that temperature overnight. The reaction mixture was then distilled under reduced pressure to remove the low-boiling fraction and the residue was diluted with 50 g of diethyl ether. Following the addition of 4 g of anhydrous calcium chloride, hydrogen chloride gas was bubbled into the mixture at room temperature for 10 minutes. Then, 5 g of anhydrous potassium carbonate were added and the mixture was thoroughly stirred. The diethyl ether solution was taken, washed with water, dried over anhydrous magnesium sulfate and distilled under reduced pressure to remove the low-boiling fraction. By the above procedure there were obtained 9.0 g of ethyl 2-isopropyl-3-formyl-propionate (general formula [XII] wherein R=--CH2CH3) yield: 89% based on ethyl α-allylisovalerate; the NMR spectrum of the aldehyde (60 MHz) δHMSCDCl3 : 9.74].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04409238
Source datasetuspto-grants-1983_10
ORD IDord-c2686a5adb414753aa6c3fedeaa8c7c6
Source noteuspto-grants-1983_10