HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → HCID 59301647, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 7-Chloro-1,3-dihydro-2H-indol-2-one | HCID 3731010 | — |
| Reactant | 1-Azulene carboxyaldehyde | HCID 11744870 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59301647 | HCID 59301647 | 57.5% |
Reaction Steps
0.3519 g 7-chlorooxindole (0.0021 mole) and 0.323 g azulene aldehyde (0.0021 mole) were dissolved in 30 mL dried ethanol. 1.5 mL pyrrolidine (1M) was then added and uniformly stirred at reflux temperature for two hours. After removal of dried ethanol, the results were extracted by dichloromethane and citric acid aqueous solution. The organic layer was collected, dried with anhydrous magnesium sulfate, filtered, concentrated under vacuum, and separated by silica gel column chromatography to give Z-form Compound 042 (0.3693 g). The total weight of 7-chlorooxindole-azulene was 0.3693 g (57.56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07714146B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-a40f02b1d8ca4044a11b755a6dc6d29c |
| Source note | uspto-grants-2010_05 |