HuagongsheHuagongshe Chemistry Print Report · For research reference only
Homoallyl bromide → N-(3-Buten-1-yl)phthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | N-(3-Buten-1-yl)phthalimide | HCID 339432 | — |
Reaction Steps
50 g (370 mmol) 4-bromo-1-butene and 68.5 g (370 mmol) phthalimide potassium salt are suspended in 800 ml ethyl methyl ketone and heated under reflux for 14 hours. After cooling, the mixture is filtrated and the filtrate is concentrated under vacuum. The residue is taken up in acetic acid ethyl ester and washed with water. The organic phase is dried over sodium sulfate and the solvent is removed under vacuum: yield 50 g (67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06903118B1 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-21fb328397d342f59110714e32a006c2 |
| Source note | uspto-grants-2005_06 |