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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methacrylic Acid | HCID 4093 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 1-Dodecanethiol | HCID 8195 | — |
| Reactant | Benzyl methacrylate | HCID 17236 | — |
| Reactant | 2-Propenamide, N-(methoxymethyl)-2-methyl- | HCID 77204 | — |
| Reactant | HCID 131729318 | HCID 131729318 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 4-[(2-Methylacryloyl)amino]benzoic acid | HCID 9859099 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076052B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-c14bdaeb89a147918a763d81c3c07300 |
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| Source note | uspto-grants-2011_12 |
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