HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isoindoline → HCID 70616527, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isoindoline | HCID 422478 | — |
| Reactant | HCID 53945814 | HCID 53945814 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70616527 | HCID 70616527 | 41% |
Reaction Steps
The process for the preparation of this compound and its physical properties will be given below. A solution of 3.46 grams of o-chlorocinnamyl chloride and 4.41 grams of isoindoline in 20 milliliters of ethanol is stirred for 12 hours at room temperature. After cmmpletion of the reaction, the solvent is distilled off. The resulting residue is then rendered alkaline by the addition of 10% sodium hydroxide and extracted with chloroform. The chloroform layer is then purified by silica gel column chromatography, and the resulting oily product is treated as in Example 1-a to obtain 2.32 grams (yield 41% of N-(o-chlorocinnamyl)-isoindoline hydrochloride as crystals having a melting point of 170°-172° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04115398 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-d0199f8c7b8f4fc59e8739c3a35b9268 |
| Source note | uspto-grants-1978_09 |