HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N-(2-cycloheptenyl)succinimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Cyclohept-2-en-1-amine | HCID 11263481 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-(2-cycloheptenyl)succinimide | HCID 13506505 | 61% |
Reaction Steps
A mixture of 2-cycloheptenylamine (1.01 g), succinic anhydride (1.0 g) and acetic acid (10 ml) was heated under reflux for 24 hours. After cooling, ether (20 ml) was added to the reaction mixture which was then washed with a saturated aqueous sodium hydrogencarbonate solution, water and a saturated aqueous sodium chloride solution in this order. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The oily product thus obtained was purified by column chromatography on silica gel to obtain 1.07 g of N-(2-cycloheptenyl)succinimide [[Compound (214)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05075488 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-5f15c2a7a5324736a1bf375111f52828 |
| Source note | uspto-grants-1991_12 |