HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Dimethylamino)ethyl methacrylate → Methacrylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Dimethylamino)ethyl methacrylate | HCID 17869 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 2-Propenoic acid, 2-methyl-, trimethylsilyl ester | HCID 2733839 | — |
| Reactant | b-Ethoxytriethylene glycol methacrylate | HCID 86746980 | — |
| Product | Methacrylic Acid | HCID 4093 | — |
| Product | (Dimethylamino)ethyl methacrylate | HCID 17869 | — |
| Product | b-Ethoxytriethylene glycol methacrylate | HCID 86746980 | — |
Reaction Steps
The solution of poly(trimethylsilyl methacrylate [48 mol %]-b-2-phenylethyl methacrylate [30 mol %]-co-2-dimethylaminoethyl methacrylate [7 mol %]-b-ethoxytriethylene glycol methacrylate [15 mol %]) was treated with 45 mL of 0.03 M methanolic tetrabutylammonium fluoride and heated at reflux for 8 hr. The solution was evaporated in a rotary evaporator under reduced pressure. The residual polymer was dried for 24 hr in a vacuum oven to give 59 g of poly(methacrylic acid [48 mol %]-b-2-phenylethyl methacrylate [30 mol %]-co-2-dimethylaminoethyl methacrylate [7 mol %]-b-ethoxytriethylene glycol methacrylate [15 mol %]). 1H NMR analysis of the product showed that no trimethylsilyl ester groups remained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05519085 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-75b0818a08fe4aeab5e5cf7c66a2af4e |
| Source note | uspto-grants-1996_05 |