Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22341Generated: October 29, 2026

4-Phenylpiperidine → 2,3-dihydro-7-methoxy-8-[2-(4-phenyl-1-piperidinyl)ethoxy]cyclopenta[c][1]benzopyran-4(1H)-one

https://huagongshe.com/reaction/22341

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenylpiperidineHCID 69873—
ReactantFumarateHCID 5460307—
Reactant2,3-dihydro-8-[2-(methanesulfonyloxy)ethoxy]-7-methoxy-cyclopenta[c][1]-benzopyran-4(1H)-oneHCID 19927716—
SolventEthanolHCID 702—
SolventIsopropanolHCID 3776—
Product2,3-dihydro-7-methoxy-8-[2-(4-phenyl-1-piperidinyl)ethoxy]cyclopenta[c][1]benzopyran-4(1H)-oneHCID 1992769293%

Reaction Steps

Method B (16 h at 60° C.); starting materials: 2,3-dihydro-8-[2-(methanesulfonyloxy)ethoxy]-7-methoxy-cyclopenta[c][1]-benzopyran-4(1H)-one (example 81) and 4-phenylpiperidine; yield 93%; fusion point 150°-152° C. (from isopropanol). Fumarate: method E; yield 84%; fusion point 185°-187° C. (from ethanol and isopropanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428038
Source datasetuspto-grants-1995_06
ORD IDord-ae92c5fb9bf44028bd0d27339139ab34
Source noteuspto-grants-1995_06