HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 86744154, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2H-1-Benzopyran-2-one, 3-acetyl-7-(diethylamino)- | HCID 688763 | — |
| Reactant | HCID 57175482 | HCID 57175482 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86744154 | HCID 86744154 | — |
Reaction Steps
To 25 mL of absolute ethanol in a 50 mL round-bottomed flask was added 217 mg (1 mmol) of 6 (N,N diethylamino) 2 formylbenzo[b]furan and 259 mg (lmmol) of 3 acetyl 7 (N,N diethylamino)coumarin. After refluxing for several minutes to dissolve the solids, 100 mg of piperidine was added and reflux was continued for one hour. The solution was allowed to cool to room temperature and then placed in a freezer overnight. The solid was filtered and recrystallized from 50 mL of ethanol to yield the product as deep red needles. Field desorption was spectrum: m/e 458 (M+); m.p. 169°-171° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04948893 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-9c2c97b70671469c821128cb3734f277 |
| Source note | uspto-grants-1990_08 |