HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl chloride → N-Allylphthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl chloride | HCID 7850 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Allylphthalimide | HCID 224401 | — |
Reaction Steps
Phthalimide potassium salt can be alkylated with allyl chloride in DMF to produce N-allylphthalimide. Under the Heck reaction conditions (Patel et al. 1977), N-allylphthalimide reacted with aryl bromide to give N-cinnamyl phthalimide. Upon treatment with hydrazine, cinnamyl amine was obtained from N-cinnamyl phthalimide (FIG. 28).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09260382B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-e64065010a6a44099b842d7b42928431 |
| Source note | uspto-grants-2016_02 |