Ethanolamine → N-(2-Hydroxyethyl)methacrylamide

To a 500 mL, four-neck round bottom flask equipped with a mechanical stirrer, a thermometer, a 200 mL dropping funnel, and a nitrogen inlet/outlet, 48.8 g of ethanolamine (0.8 moles), 80 mg of 4-methoxyphenol and 100 mL of acetonitrile were added. The mixture was cooled below 0° C. with an ice/water salt bath. To this solution, 41.8 g of freshly distilled methacryloyl chloride (0.4 mole) in 100 mL of acetonitrile was added through the dropping funnel. The addition rate was controlled so that the reaction temperature was kept below 0° C. At the end of addition, the pH of the reaction mixture was adjusted to 7 with either methacryloyl chloride or ethanolamine solution. While keeping the reaction solution cold (below 5° C.), the ethanolamine HCl salts were filtered out. To the filtrate, 200 mL of deionized water and 40 g of Dowex MR-3C resin, which was pre-washed with two bed volumes of 1/1 ratio acetonitrile/water mixture for three times, were added. The resin was removed by filtration after agitating for one hour. The filtrate was concentrated to about 160 g by vacuum distillation. The final solution has the following properties: HPLC and FT-IR analysis indicates there is no ester formation; HEMAA concentration: 23.5% (wt/wt); pH=6.9 at 250° C.; Conductivity=3.9 μS/cm at 25° C.; Viscosity=1.9 cPs at 25° C. The yield of HEMAA was about 73%.

1. customTo a 500 mL, four-neck round bottom flask equipped with a mechanical stirrer
2. temperatureThe mixture was cooled below 0° C. with an ice/water salt bath
3. customwas kept below 0° C
4. additionAt the end of addition
5. customthe reaction solution cold (below 5° C.)
6. filtrationthe ethanolamine HCl salts were filtered out
7. washTo the filtrate, 200 mL of deionized water and 40 g of Dowex MR-3C resin, which was pre-washed with two bed volumes of 1/1 ratio acetonitrile/water mixture for three times
8. additionwere added
9. customThe resin was removed by filtration
10. concentrationThe filtrate was concentrated to about 160 g by vacuum distillation
11. customat 250° C.
12. customat 25° C.
13. customat 25° C

ORDレコード

ord-dc635dc431a94ab39dafb7c160343b49

出典データセット

uspto-grants-2002_10

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06464850B1