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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35980Generated: October 26, 2026

Methacrylic anhydride → 2-Hydroxypropyl carbamate methacrylate

https://huagongshe.com/reaction/35980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethacrylic anhydrideHCID 12974—
Reactant1,2-Propanediol, monocarbamateHCID 243575—
Catalyst2-Methoxybenzene-1,4-diolHCID 69988—
SolventPyridineHCID 1049—
Product2-Hydroxypropyl carbamate methacrylateHCID 1993966567.2%

Reaction Conditions

Temperature65 °C

Reaction Steps

A four-necked, five-liter round-bottomed reaction flask equipped with a thermometer, condenser, mechanical stirrer, and air sparger is charged with 1,920 g (16.1 moles) of 2-hydroxypropyl carbamate, 2,236 g (14.5 moles) of distilled methacrylic anhydride, 83 g of anhydrous pyridine, and 4.2 g (1,000 parts per million) methoxyhydroquinone. The reaction mass is stirred and slowly heated to 65° C. with a hot-water bath. During this heating period and during the course of the reaction, the reaction mass is sparged with air. The reaction mass is held at 65° C. until the concentration of methacrylic anhydride decreased to less than 1.5 percent by weight. The resulting product is then washed with a saturated solution of sodium carbonate, and the aqueous layer removed from the solids by decantation. This washing procedure is repeated two more times to neutralize all of the methacrylic acid. The resulting solid product is then washed twice with a total of two gallons of distilled water. For each wash, the solids are melted by heating the wash water to 50° C. During the washing procedure, the melted solids are well stirred and the aqueous material is allowed to separate from the molten organic material and decanted before the desired product resolidifies. The wet product is dried overnight in a hood to yield 2,000 g of anhydrous 2-hydroxypropyl carbamate methacrylate that analysis indicates has a 97% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05412049
Source datasetuspto-grants-1995_05
ORD IDord-ed1f1e4e7c1e40bba5e764fad94c5985
Source noteuspto-grants-1995_05