HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(Piperidin-3-yl)-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Piperidin-3-amine | HCID 148119 | — |
| Reactant | 1-(2-Carboxybenzoyl)-3-phthalimidopiperidine | HCID 21482812 | — |
| Product | 2-(Piperidin-3-yl)-1H-isoindole-1,3(2H)-dione | HCID 19972263 | — |
Reaction Steps
A mixture of 10 g. of 3-aminopiperidine and 29.6 g. of phthalic anhydride is heated at 150° C. for 30 minutes. This mixture which contains 1-(2-carboxybenzoyl)-3-phthalimidopiperidine is heated at reflux with 500 ml. of 6N hydrochloric acid for two hours. The aqueous phase is extracted with ether and then concentrated in vacuo. The residue is extracted with dilute aqueous sodium hydroxide solution and methylene chloride. The organic phase is dried and concentrated in vacuo to give 3-phthalimidopiperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04005208 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-f8757a0ce6bb4892ae6327e0a4d9eeb0 |
| Source note | uspto-grants-1977_01 |