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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526805Generated: October 25, 2026

Acetoin → HCID 19357483, compound

https://huagongshe.com/reaction/526805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoinHCID 179—
ReactantTriethylamineHCID 8471—
ReactantMethacryloyl chlorideHCID 13528—
Catalyst4-MethoxyphenolHCID 9015—
SolventDichloromethaneHCID 6344—
ProductHCID 19357483HCID 1935748353.1%

Reaction Conditions

Temperature5 °C

Reaction Steps

In a 2 L four-necked flask subjected replacement with nitrogen, 150 g of 3-hydroxy-2-butanone (made by Tokyo Chemical Industry Co., Ltd., purity: 95.0% or more) was put, and dissolved in 750 g of methylene chloride, and a stirrer, a thermometer and a Dimroth cooling tube were connected thereto. After the solution was stirred and cooled to about 5° C., 190 g of triethylamine and 80 mg of p-methoxyphenol were added thereto. While the solution was cooled to about 5° C. under stirring, 178 g of methacryloyl chloride was slowly added dropwise thereto over 4 hours, and further stirred for 30 minutes after completion of the dropwise addition to allow a reaction. The resulting reaction mixture was washed with 1 N-hydrochloric acid, a 10% sodium carbonate aqueous solution and saturated brine at room temperature, dried over anhydrous magnesium sulfate and separated by filtration to obtain a reaction crude liquid. The solvent of the reaction crude liquid was distilled off using an evaporator, 80 mg of p-methoxyphenol was added thereto and the resulting solution was distilled under reduced pressure to give 141 g of 3-oxobutane-2-yl methacrylate of 96.5% GC purity (yield: 53.1% based on 3-hydroxy-2-butanone).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346775B2
Source datasetuspto-grants-2016_05
ORD IDord-33fe739cceb54b13a9279ebb70c7a281
Source noteuspto-grants-2016_05