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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 721964Generated: October 29, 2026

Piperidine → HCID 69535235, compound

https://huagongshe.com/reaction/721964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantPhenylsulphonylacetonitrileHCID 82077—
Reactant4-[(2-Methylprop-2-en-1-yl)oxy]benzaldehydeHCID 13203751—
SolventEthanolHCID 702—
ProductHCID 69535235HCID 6953523577%

Reaction Steps

A solution of 4-(2-methylallyloxy)-benzaldehyde (7.03 g, 40 mmol) and of (phenylsulfonyl)acetonitrile (7.24 g, 40 mmol) in 70 ml absolute ethanol is heated under reflux in the presence of a catalytic quantity of piperidine (0.5 ml) for 48 hours. The reaction medium is cooled to room temperature and the precipitate formed is filtered and washed with cold ethanol. After drying in a dessicator, 10.45 g (yield 77%) of 2-benzenesulfonyl-3-[4-(2-methylallyloxy)phenyl]acrylonitrile are obtained in the form of a very pale yellow solid which is used as it is in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138108B2
Source datasetuspto-grants-2006_11
ORD IDord-6b89454ad4cb48a09e5a8b203db011a3
Source noteuspto-grants-2006_11