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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417207Generated: October 25, 2026

Piperidine → Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-5-fluoro-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/417207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant3-Chloro-2-fluorobenzaldehydeHCID 736335—
Reactant6-Chloro-5-fluoroindolin-2-oneHCID 9794083—
SolventMethanolHCID 887—
ProductZ-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-5-fluoro-1,3-dihydro-indol-2-oneHCID 8665393387%

Reaction Conditions

Temperature50 °C

Reaction Steps

To the mixture of 6-chloro-5-fluoroindolin-2-one (Natrochem) (2.88 g, 15.5 mmol) and 3-chloro-2-fluorobenzaldehyde (3.69 g, 23.3 mmol) (Aldrich) in methanol (140 mL) was added piperidine (3.96 g, 46.6 mmol) (Aldrich) dropwise. The mixture was then heated at 50° C. for 3 h. After cooled to 4° C., the mixture was filtered and resulting precipitate was collected, dried to give E/Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-5-fluoro-1,3-dihydro-indol-2-one as a yellow solid (Yield 4.4 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088815B2
Source datasetuspto-grants-2012_01
ORD IDord-d6579ea61160444eb895eee759c569ed
Source noteuspto-grants-2012_01