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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611725Generated: October 26, 2026

Sulfuric Acid → Butyl prop-2-enoate--methyl 2-methylprop-2-enoate (1/1)

https://huagongshe.com/reaction/611725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantMethyl MethacrylateHCID 6658—
Reactant1-DodecanethiolHCID 8195—
ReactantButyl AcrylateHCID 8846—
ReactantPotassium PersulfateHCID 24412—
SolventWaterHCID 962—
ProductButyl prop-2-enoate--methyl 2-methylprop-2-enoate (1/1)HCID 62802—

Reaction Conditions

Temperature70 °C

Reaction Steps

A glass-made vessel equipped with a reflux condenser, a dropping funnel, a thermometer, a nitrogen blowing-in nozzle and a stirrer was charged with 5 parts of PVA having a mercapto group at only one end thereof (PVA-3: degree of polymerization of 550, degree of hydrolysis of 88.3 mol %, mercapto group content of 3.3×10-5 equivalent/g) and 90 parts of ion-exchanged water, and the PVA was completely dissolved in the water at 95° C. The resultant aqueous solution of the PVA was adjusted to pH=4 with dilute sulfuric acid, and incorporated, under stirring at 150 r.p.m., with 10 parts of methyl methacrylate, 10 parts of n-butyl acrylate and 0.1 part of n-dodecyl mercaptan. Then, the reaction system was replaced with nitrogen, and the temperature in the system was raised to 70° C. Subsequently, emulsion polymerization was initiated by adding to the system, 5 parts of aqueous solution of potassium persulfate having a concentration of 1%. To the system were continuously added the mixture of 40 parts of methyl methacrylate, 40 parts of n-butyl acrylate and 0.4 part of n-dodecyl mercaptan over a period of 2 hours. The polymerization was finished at the time when a conversion of 99.5% was achieved after 3 hours from the start of the polymerization. As a result, there was obtained a stable emulsion of methyl methacrylate/n-butyl acrylate copolymer having a solid concentration of 52.0%. Thereafter, the procedure in Example 1 was repeated to produce the synthetic resin powder except that the emulsion thus obtained was used. The results of evaluation of the powder are given in Tables 3 and 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06001903
Source datasetuspto-grants-1999_12
ORD IDord-b956cc9a74984f7cbc4d6df830b542e6
Source noteuspto-grants-1999_12