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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22042Generated: October 23, 2026

Acrylic Acid → 1-Butanaminium, N,N,N-tributyl-, 2-propenoate (1:1)

https://huagongshe.com/en/reaction/22042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylic AcidHCID 6581—
ReactantTetrabutylammonium HydroxideHCID 2723671—
Product1-Butanaminium, N,N,N-tributyl-, 2-propenoate (1:1)HCID 3014922—

Reaction Conditions

Temperature65 °C

Reaction Steps

A 5 liter glass reaction vessel, fitted with a magnetic stirrer, a hose connector, and a septum were purged with nitrogen. Operating in an atmosphere of nitrogen, 297 grams of poly(isobutylene-co-parabromomethylstyrene) (Mv=1.2M, 1.7% para-bromomethylstyrene) was placed into the vessel along with 3.5 liters of xylenes. The polymer was dissolved with stirring under a partial vacuum of 100 mm Hg with a nitrogen sparge attached at the bottom of the solution. A xylene solution of tetrabutylammonium acrylate was prepared in a second flask under nitrogen by placing 100 ml xylenes, 60 ml tetrabutylammonium hydroxide (1M in methanol) and 6.0 g acrylic acid together with stirring. The contents of the flask was concentrated to half its volume and then diluted to 0.5 liters with more xylenes. This solution was then added to the flask containing the poly(isobutylene-co-para-bromomethylstyrene) and the temperature of the solution was raised to 65° C. The reaction was complete in six hours and the polymer was isolated by precipitation in isopropanol. The polymer was dried in a vacuum oven at 1 mm Hg, 40° C. The analysis for the acrylate content (FTIR and NMR) indicate that the modified polymer has 0.24 meq/gram which is consistent with the complete conversion of acrylic acid to acrylic ester and total conversion of the benzylbromide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05426167
Source datasetuspto-grants-1995_06
ORD IDord-687d7e275b804438aca088ce635be0aa
Source noteuspto-grants-1995_06