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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651495Generated: October 25, 2026

Isopropanol → Acrylic Acid 1-allyloxy-2-propanol

https://huagongshe.com/reaction/1651495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantAcrylic AcidHCID 6581—
ReactantSodium PersulfateHCID 62655—
Reactant2-Propanol, 1-(2-propenyloxy)-HCID 542178—
SolventWaterHCID 962—
ProductAcrylic Acid 1-allyloxy-2-propanolHCID 86743966—

Reaction Conditions

Temperature40 °C

Reaction Steps

A suitable reaction flask was equipped with a mechanical agitator, a thermometer, a reflux condenser, a nitrogen inlet and two addition inlets for the initiator and monomer solutions. The flask was charged with 170 g of deionized water and 30 g of isopropanol. The resulting solution was then heated to reflux under a nitrogen blanket. 43.2 g of acrylic acid (0.6 mole) and 23.2 g of 1-allyloxy-2-propanol [AOP] (94% pure, 0.19 mole) were mixed in a separate flask so as to provide a mixed monomer solution. The mixed monomer solution was then transferred to an addition funnel. An initiator solution containing 24.4% of sodium persulfate in deionized water was prepared separately and sparged with nitrogen. The initiator solution (17 g) was then added to the reaction flask along with the mixed monomer solution over a period of two hours. After this addition, some addition persulfate solution was added to the reaction mixture for one more hour at 85° C. and, subsequently, 90.0 g of the isopropanol/water solution were stripped off. The reaction mixture was then cooled to lower than 40° C. and 36 g of 50% caustic solution was then added.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929362
Source datasetuspto-grants-1990_05
ORD IDord-ea64ae1bd84b4b06aca3fb4ef81f8b1b
Source noteuspto-grants-1990_05