HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → N-(1-phenylcyclopropyl)-alpha-bromo-tert-butylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | 1-Phenyl-cyclopropylamine | HCID 194549 | — |
| Reactant | 2-Bromo-3,3-dimethylbutanoyl chloride | HCID 10867621 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | N-(1-phenylcyclopropyl)-alpha-bromo-tert-butylacetamide | HCID 12760535 | 71.4% |
Reaction Steps
Into a 200 ml four-necked flask, there were charged benzene (100 ml), 1-phenylcyclopropylamine (8.9 g) and triethylamine (7.4 g), and α-bromo-tert-butylacetyl chloride (14.5 g) was dropwise added thereto while stirring at room temperature. Stirring was continued for 3 hours. After completion of the reaction, the reaction mixture was washed with water to remove triethylamine hydrochloride. The benzene layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was recrystallized from ethanol to give 14.8 g of N-(1-phenylcyclopropyl)-α-bromo-tert-butylacetamide. M.P., 161°-162.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04288244 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-a7189525640c4b379108d7190376d22a |
| Source note | uspto-grants-1981_09 |