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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606332Generated: October 30, 2026

Piperidine → HCID 86733278, compound

https://huagongshe.com/reaction/1606332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 126440HCID 126440—
SolventEthanolHCID 702—
ProductHCID 86733278HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952104
Source datasetuspto-grants-1976_04
ORD IDord-1b7b0fc3c68a407182c01185e31175de
Source noteuspto-grants-1976_04