HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Bromo-1-heptene → N-(hept-6-enyl)phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Bromo-1-heptene | HCID 524450 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(hept-6-enyl)phthalimide | HCID 53236045 | — |
Reaction Steps
A solution of potassium phthalimide (627 mg, 3.38 mmol) and 7-bromohept-1-ene in dry DMF (10 mL) was stirred at 100° C. under nitrogen for 1 h. Then, the reaction mixture was successively cooled to room temperature, filtered, diluted with ether, and filtered again. The filtrate was concentrated under reduced pressure to give the target product 75 as an oil, which was used without further purifications in the next step: m/z=244 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08741926B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-523896de0abd4407a2547d80ef65f7c7 |
| Source note | uspto-grants-2014_06 |