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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786535Generated: October 29, 2026

Piperidine → HCID 9824560, compound

https://huagongshe.com/reaction/1786535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant5,6,7,8-Tetrahydro-1-naphtholHCID 68258—
ReactantHCID 3773318HCID 3773318—
SolventEthanolHCID 702—
ProductHCID 9824560HCID 98245601.4%

Reaction Steps

To a stirred suspension of 3,4-dimethoxy-5-bromobenzylidenemalononitrile (293 mg, 1 mmol) and 5,6,7,8-Tetrahydro-1-naphthol (148 mg, 1 mmol) in ethanol (4 ml) was added piperidine (0.1 ml, 1 mmol), and the mixture was refluxed for 2 h. The solvent was evaporated and the residue was purified by column chromatography (EtOAc/Hexane, 1:2), yielding the title compound (6 mg, 1.4%). 1H NMR (CDCl3): 7.89 (d, J=2.0, 1H), 6.80-6.69 (m, 3H), 4.63 (s, 3H), 3.86 (s, 3H), 3.83 (s, 3H), 2.72 (m, 4H), 1.8 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507762B2
Source datasetuspto-grants-2009_03
ORD IDord-38a4490365184c17bf9ebd83390c64c8
Source noteuspto-grants-2009_03