HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(4-Bromophenyl)-N-methyl-3-methyl-2-butenamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Methyl-2-butenoyl chloride | HCID 102394 | — |
| Reactant | Benzenamine, 4-bromo-N-methyl- | HCID 2757052 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-Bromophenyl)-N-methyl-3-methyl-2-butenamide | HCID 22568913 | — |
Reaction Steps
3,3-Dimethylacryloyl chloride (3 mL, 27 mmol) was added to a solution of 4-bromo-N-methyl-aniline (4.55 g, 25 mmol) in 150 mL of dichloromethane followed after 5 minutes by triethyl amine (5 mL, 33 mmol). After 2.5 h at ambient temperature, the reaction mixture was washed with water and the organic phase was dried over anhydrous sodium sulfate and evaporated in vacuo to afford the title product as a brown oil in quantitative yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06855512B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-90623539d9304fb8841d096e490d9518 |
| Source note | uspto-grants-2005_02 |