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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941012Generated: October 31, 2026

Acrylic Acid → Prop-2-enoic acid--6-methylheptyl prop-2-enoate (1/1)

https://huagongshe.com/reaction/1941012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylic AcidHCID 6581—
ReactantBenzoyl PeroxideHCID 7187—
ReactantIsooctyl acrylateHCID 165746—
SolventEthyl AcetateHCID 8857—
SolventHeptaneHCID 8900—
ProductProp-2-enoic acid--6-methylheptyl prop-2-enoate (1/1)HCID 165745—

Reaction Conditions

Temperature60 °C

Reaction Steps

A flask equipped with an agitator, condenser, nitrogen inlet tube and an addition funnel is charged with isooctyl acrylate (72.0 g), acrylic acid (8.0 g) and ethyl acetate (78.1 g). The mixture is heated to 60° C. with medium agitation and purged with nitrogen to remove oxygen. Lucidol 75 (0.07 g, available from Elf Atochem North America) premixed in ethyl acetate (3.0 g) is added to initiate reaction. The reaction temperature is maintained at 60° C. Ethyl acetate (1.5 g) is added to the polymer solution every 30 minutes until the conversion of isooctyl acrylate to polymer reaches a minimum of 95%, typically 20-30 hours. An additional charge of Lucidol 75 (0.07 g) premixed with ethyl acetate (3.0 g) is added after 5 hours and nine hours reaction time. When 95% minimum reaction conversion is achieved, the resulting polymer solution is diluted with heptane to 20-23% solids, cooled and drained. The inherent viscosity in ethyl acetate at 0.15 g,/dl is measured at 1.7-2.0 dl/g. The inherent viscosity is measured by conventional means using a Canon-Fenske #50 viscometer in a water bath controlled at 27° C. to measure the flow time of 10 milliliters of the polymer solution. The test procedure and apparatus are described in detail in "Textbook of Polymer Science", F. W. Billmeyer, Wiley Interscience, Second Edition, 1971, pages 84 and 85.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05702720
Source datasetuspto-grants-1997_12
ORD IDord-04a15e5605df463a8b18e3f25bc4b57b
Source noteuspto-grants-1997_12