HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054571Generated: October 30, 2026
Methyl iodide → Poly(oxy-1,2-ethanediyl), α-methyl-ω-[2-[(1-oxo-2-propen-1-yl)amino]ethoxy]-
https://huagongshe.com/reaction/2054571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 19364541 | HCID 19364541 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Poly(oxy-1,2-ethanediyl), α-methyl-ω-[2-[(1-oxo-2-propen-1-yl)amino]ethoxy]- | HCID 61849582 | — |
Reaction Steps
N-[2-(2-hydroxyethoxy)ethyl]acrylamide (35.87 g), potassium hydroxide (15.2 g), tetrahydrofuran (100 g) and methyl iodide (33.58 g) were introduced into a 1 L eggplant type flask equipped with a reflux condenser and a magnetic rotor. A reaction was carried out at 45° C. for 2 hours and then for 2 hours at 60° C. as the mixture was being stirred. The salt that separated out was removed by filtration and the low boiling point components were removed by means of a rotary vacuum evaporator. Purification was performed by distillation under reduced pressure and N-[2-(2-methoxyethoxy)ethyl]acrylamide was obtained as a yellow transparent, viscous liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07329694B2 |
|---|
| Source dataset | uspto-grants-2008_02 |
|---|
| ORD ID | ord-3ed0b7e229d8429baa4f38b435f191b5 |
|---|
| Source note | uspto-grants-2008_02 |
|---|