Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657458Generated: October 29, 2026

Methacrylic Acid → 4-[(2-Methylacryloyl)amino]benzoic acid

https://huagongshe.com/reaction/657458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethacrylic AcidHCID 4093—
ReactantAzobisisobutyronitrileHCID 6547—
Reactant1-DodecanethiolHCID 8195—
ReactantBenzyl methacrylateHCID 17236—
Reactant2-Propenamide, N-(methoxymethyl)-2-methyl-HCID 77204—
ReactantHCID 131729318HCID 131729318—
Solvent2-MethoxyethanolHCID 8019—
Product4-[(2-Methylacryloyl)amino]benzoic acidHCID 9859099—

Reaction Conditions

Temperature80 °C

Reaction Steps

Methyl cellosolve (199.8 g), N-methoxymethyl methacrylamide (18 g), benzyl methacrylate (11.4 g), methacrylic acid (3 g), dodecyl mercaptan (0.075 g), and Vazo-64 (0.6 g) were added to 500 ml 4-neck ground glass flask, equipped with a heating mantle, temperature controller, mechanical stirrer, condenser, pressure equalized addition funnel and nitrogen inlet. The reaction mixture was heated to 80° C. under nitrogen atmosphere. Then, a pre-mixture of N-methoxymethyl methacrylamide (55 g), benzyl methacrylate (34 g), methacrylic acid (9 g), dodecyl mercaptan (0.225 g), and Vazo-64 (1.2 g) were added over two hours at 80° C. The reaction was continued another eight hours and Vazo 64 (0.35 g) was added two more times. The polymer conversion was >99% based on determination of percent of non-volatiles. The weight ratio of N-methoxymethyl methacrylamide/benzyl methacrylate/methacrylic acid in the polymer was 56/34.8/9.2. The resin solution was precipitated in powder form using DI water/Ice (3:1) and a Lab Dispersator (4000 RPM) and then filtered. The resulting powder was dried at room temperature for 24 hours. The next day, a tray containing the polymer was placed in oven at 110° F. (43° C.) for two additional days. The yield was 95% and polymer acid number was 58 (actual) versus 58.8 (theoretical).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08076052B2
Source datasetuspto-grants-2011_12
ORD IDord-c14bdaeb89a147918a763d81c3c07300
Source noteuspto-grants-2011_12