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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727954Generated: November 3, 2026

Piperidine → Z-6-chloro-3-cyclopentylmethylene-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1727954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantCyclopentanecarbaldehydeHCID 70106—
Reactant6-Chloro-1,3-dihydroindol-2-oneHCID 736344—
SolventMethanolHCID 887—
ProductZ-6-chloro-3-cyclopentylmethylene-1,3-dihydro-indol-2-oneHCID 68614585—

Reaction Steps

In a manner similar to the method described in example 1a, 6-chlorooxindole (1.16 g, 6.59 mmol) was reacted with cyclopentanecarbaldehyde (0.77 g, 7.85 mmol) (Wiley) and piperidine (0.67 g, 7.85 mmol) in methanol to give a mixture of E- and Z-6-Chloro-3-cyclopentylmethylene-1,3-dihydro-indol-2-one as a brown oil (Yield 0.8 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495007B2
Source datasetuspto-grants-2009_02
ORD IDord-f72d12984670483e87f41499dc8e29de
Source noteuspto-grants-2009_02