HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 86733278, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 126440 | HCID 126440 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86733278 | HCID 86733278 | — |
Reaction Steps
A solution of 5 parts of 8-allyl-5-(3-methyl-n-butoxy)-4-oxo-4H-1-benzopyran-2-carboxylic acid and 1.35 parts of piperidine in 50 parts of ethanol was refluxed for 2 hours. The resulting solution was filtered and evaporated to an oil which was dissolved in dry benzene. The benzene solution was evaporated to give an oil which was triturated with petroleum ether (b.p. 40°-60° C) to give 6 parts of 8-allyl-5-(3-methyl-n-butoxy)-4-oxo-4H-1-benzopyran-2-carboxylic acid piperidine salt as a white solid m.p. 106°-107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03952104 |
| Source dataset | uspto-grants-1976_04 |
| ORD ID | ord-1b7b0fc3c68a407182c01185e31175de |
| Source note | uspto-grants-1976_04 |