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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190103Generated: November 1, 2026

3-Fluoro-p-anisaldehyde → HCID 68617947, compound

https://huagongshe.com/reaction/2190103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-p-anisaldehydeHCID 67696—
ReactantIndol-2-oneHCID 17904787—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 68617947HCID 68617947—

Reaction Steps

A mixture of 1.33 g of indole-2-one (10 mmol), 1.54 g of 3-fluoro-4-methoxybenzaldehyde (10 mmol) and 3 drops of piperidine are refluxed in 40 ml of ethanol for 5 hours. The desired product precipitates as a yellow crystalline solid during the reaction. After cooling to room temperature, the product is filtered off, washed with ethanol and dried in vacuo. Yield 2.2 g (82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324267B2
Source datasetuspto-grants-2012_12
ORD IDord-5c232a12e65d488099c79f5e63dbb933
Source noteuspto-grants-2012_12