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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22316Generated: October 25, 2026

tert-Butyl methyl ether → 6-(1-methylethoxy)-7-[3-(4-phenyl-1-piperidinyl)propoxy]-2H-1-benzopyran-2-one

https://huagongshe.com/reaction/22316

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl methyl etherHCID 15413—
Reactant4-PhenylpiperidineHCID 69873—
ReactantFumarateHCID 5460307—
Reactant7-[3-(methanesulfonyloxy)propoxy]-6-(1-methylethoxy)-2H-1-benzopyran-2-oneHCID 19927700—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
Product6-(1-methylethoxy)-7-[3-(4-phenyl-1-piperidinyl)propoxy]-2H-1-benzopyran-2-oneHCID 1992772269%

Reaction Steps

Method B (24 h at 60° C.); starting materials: 7-[3-(methanesulfonyloxy)propoxy]-6-(1-methylethoxy)-2H-1-benzopyran-2-one (example 73) and 4-phenylpiperidine; yield 69%; fusion point 86°-87° C. (from TBME). Fumarate: method E; yield 90%; fusion point 164°-167° C. (from ethanol and acetone).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428038
Source datasetuspto-grants-1995_06
ORD IDord-839f4529654e48c7bbcee0290e2694f8
Source noteuspto-grants-1995_06