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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973905Generated: October 25, 2026

Benzoic Acid → Vinylbenzoic acid

https://huagongshe.com/reaction/973905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantNitrogenHCID 947—
ReactantAllyl methacrylateHCID 7274—
ReactantLauryl MethacrylateHCID 8906—
Reactant4-Vinylbenzoic acidHCID 14098—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductVinylbenzoic acidHCID 3015504—

Reaction Conditions

Temperature70 °C

Reaction Steps

Into a 500 ml. 2-necked flask fitted with a thermometer, and a reflux condenser connected to a N2 source, was introduced a mixture of 3.5 g of 4-vinylbenzoic acid (Aldrich Chemical Co. , 3 g of allyl methacrylate, 150 ml tetrahydrofuran and 150 ml ethylacetate. The mixture was stirred to dissolve the benzoic acid compound. Next was added 93.5 g of laurylmethacrylate. The flask was purged with N2 and heated at 70° C. for 10 minutes. The flask was purged again with N2 and 1 g of 2,2-azobisisobutyronitrile (AIBN) was added all at once and heated at 70° C. under a N2 blanket. This was continued for a period of 8 hours. The resulting polymeric solution was cooled to room temperature and diluted with twice its volume with Isopar™ G and filtered to remove insoluble materials (About 125 mg of homopolymer of VBA acid remained on the filter paper). The clear filtered polymeric solution was further diluted with Isopar™ G to 4.1 liters and was subjected to distillation under reduced pressure until about 500 ml of the distillate was collected in the receiving flask. The distillate was mainly ethylacetate, tetrahydrofuran and Isopar™ G).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05066559
Source datasetuspto-grants-1991_11
ORD IDord-f4a56db9433e4313ac9b26d3334542cb
Source noteuspto-grants-1991_11