HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → N-(2-cycloheptenyl)dichloromaleinimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dichloromaleic anhydride | HCID 70728 | — |
| Reactant | Cyclohept-2-en-1-amine | HCID 11263481 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-(2-cycloheptenyl)dichloromaleinimide | HCID 13578660 | 70.7% |
Reaction Steps
A mixture of 2-cycloheptenylamine (1.01 g), dichloromaleic anhydride (1.67 g) and acetic acid (10 ml) was heated under reflux for 3 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 deposited crystal was purified by recrystallization from hexane to obtain 1.67 g of N-(2-cycloheptenyl)dichloromaleinimide [Compound (217)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04709052 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-abdfc592559a4f5aa99b7d586c93a409 |
| Source note | uspto-grants-1987_11 |