HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-Methyl-N-propylprop-2-enamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acetimidate | HCID 21947001 | — |
| Reactant | 3-Aminopropyl methacrylamide hydrochloride | HCID 86600969 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Methyl-N-propylprop-2-enamide | HCID 9793765 | 92% |
Reaction Steps
0.8 g of 3-aminopropyl methacrylamide hydrochloride was dissolved in a methanol solvent and 0.9 g of acetic 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 acetylamide, N-3-propyl methacrylamide (yield: 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06956077B1 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-ef9454bd0e574f18b49a30f89cd8c813 |
| Source note | uspto-grants-2005_10 |