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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393482Generated: October 29, 2026

Catechol → 1'-ethoxycarbonyl-spiro[1,3-benzodioxole-2,4'-piperidine]

https://huagongshe.com/reaction/2393482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCatecholHCID 289—
ReactantWaterHCID 962—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantEthyl 4-oxo-1-piperidinecarboxylateHCID 34767—
SolventTolueneHCID 1140—
Product1'-ethoxycarbonyl-spiro[1,3-benzodioxole-2,4'-piperidine]HCID 10445457—

Reaction Steps

A mixture of 1-ethoxycarbonyl-4-piperidinone (17 g), pyrocatechol (13 g) and p-toluenesulfonic acid (2.5 g) in 250 ml of dry toluene was refluxed with continous removal of water. After 3 h the reaction mixture was concentrated in vacuo , 2% NaOH (200 ml) was added followed by extraction with dichloromethane. After drying over magnesium sulfate and removal of solvent in vacuo, the remaining red oil was applied to a silica gel column (eluent: ethyl acetate/heptane=1:1) giving 22 g of a slightly yellow oil, 1'-ethoxycarbonyi-spiro[1,3-benzodioxole-2,4'-piperidine].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807871
Source datasetuspto-grants-1998_09
ORD IDord-e046ea28e1774d90ae3ac7d4d1ed6285
Source noteuspto-grants-1998_09