HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Propionamide propyl methacrylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propionic anhydride | HCID 31263 | — |
| Reactant | 3-Aminopropyl methacrylamide hydrochloride | HCID 86600969 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Propionamide propyl methacrylamide | HCID 86600968 | 95% |
Reaction Steps
0.8 g of 3-aminopropyl methacrylamide hydrochloride was dissolved in a methanol solvent and 1.0 g of propionic anhydride and 0.9 g of triethylamine (TEA) were added thereto. The resultant mixture was stirred under ice-cooling for 4 hours. After the completion of the reaction, the solvent was distilled off with an evaporator and the precipitate was filtered off. The filtrate was recovered and introduced into a silica column. Thus, the eluate fraction containing the target product was taken up and subjected to recrystallization to thereby purify the target propionamide-propyl methacrylamide (yield: 95%). FIG. 2 shows the result of the mass spectrometry of the purified product while FIG. 3 shows the result of 1H-NMR thereof.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06956077B1 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-b22b9ba3f0b24ca0904a746381ae6e14 |
| Source note | uspto-grants-2005_10 |