HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-methyl-N-(3-bromophenyl)-3,3-dimethyl-acrylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-3,3-Dimethylacryloyl-3-bromoaniline | HCID 19177475 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N-methyl-N-(3-bromophenyl)-3,3-dimethyl-acrylamide | HCID 19935491 | 85.2% |
Reaction Steps
28.7 g of powdered potassium hydroxide were suspended in 300 ml of dimethyl sulfoxide and a solution of 32.6 g of N-(3-bromophenyl)-3,3-dimethyl-acrylamide in 200 ml of dimethylsulfoxide (DMSO) was added dropwise thereto. The mixture was stirred at room temperature for 30 minutes and subsequently a solution of 27.5 g of methyl iodide in 150 ml of DMSO was added dropwise thereto. After 2.5 hours the mixture was poured on to 1 1 of ice/water and extracted with ethyl acetate. The organic phase was washed repeatedly with water, dried and evaporated. The oily residue was distilled in a high vacuum. There were obtained 29.3 g of N-methyl-N-(3-bromophenyl)-3,3-dimethyl-acrylamide as a slightly yellow oil, boiling point 112°-114° C./67 Pa.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05037825 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-d7dbc54b4ea64204b0deaa7876a4c0d5 |
| Source note | uspto-grants-1991_08 |