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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207855Generated: November 2, 2026

Methyl Acrylate → HCID 86658588, compound

https://huagongshe.com/reaction/2207855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantPropyleneHCID 8252—
ProductHCID 86658588HCID 86658588—

Reaction Steps

Subsequently, the inside of an induction stirring-type stainless steel-made autoclave having an inner volume of 2 liters for use in the polymerization was purged with purified nitrogen, and purified toluene (500 mL), methyl acrylate (37.5 mL) and the entire amount of the catalyst slurry prepared above were introduced into the autoclave in a purified nitrogen atmosphere. Propylene (100 mL) was introduced into the autoclave at 20° C., and the mixed gas prepared above was introduced to raise the pressure to 1.2 MPa. Thereafter, the temperature was raised to 55° C., and the mixed gas was added so that the total pressure could become 2.0 MPa. The mixed gas was appropriately introduced to keep the total pressure during the polymerization. After 25 minutes, ethanol (25 ml) was charged, and the unreacted gas was purged, thereby stopping the polymerization. The recovered toluene suspension was added with ethanol (1,000 mL), and the mixture was left standing still for one night and then filtered. Acetone (500 mL) was added to the precipitate and after stirring at 20° C. for 20 minutes, filtration was performed. This washing was performed two more times. After the washing, the polymer was dried under reduced pressure at 70° C. for 3 hours to obtain 19.6 g of an ethylene-propylene-methyl acrylate copolymer (catalytic activity: 8.1E+04 (g/mol/h)). The melting point by DSC of the obtained copolymer was 113.6° C., Mw by GPC was 58,000, Mw/Mn was 1.6, the methyl acrylate content was 0.6 mol %, and the propylene content was 2.4 mol %. The polymerization results are shown in Table 12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376459B2
Source datasetuspto-grants-2016_06
ORD IDord-c450dad8c8e840ddb03d2f4a6edfbfd5
Source noteuspto-grants-2016_06