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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839528Generated: November 2, 2026

4-Hydroxybenzaldehyde → HCID 9837407, compound

https://huagongshe.com/reaction/1839528

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantSodium HydroxideHCID 14798—
Reactant3-PyridineacetonitrileHCID 80923—
SolventMethanolHCID 887—
ProductHCID 9837407HCID 983740766%

Reaction Steps

A mixture of 4-hydroxybenzaldehyde (0.5 g, 4.1 mmoles), 3-pyridylacetonitrile (0.54 ml, 4.1 mmoles) and 50% w/v of aqueous NaOH (3.3 ml) in methanol (10 ml) was stirred at room temperature for 30 minutes. The yellow precipitate that formed was filtered, washed with cooled methanol (1 ml), cooled CH2Cl2 (10 ml), and dried under vacuum over P2O5 to yield 0.6 g (66%) of the title compound. 1H-NMR (CD3OD) 8.8 (d, 1H), 8.4 (m, 1H), 8.05 (m, 1H), 7.8 (m, 2H), 7.6 (s, 1H), 7.4 (m, 1H), 6.6 (m, 2H). 13C-NMR (DMSO) 177.52, 175.57, 146.59, 145.06, 144.78, 133.15, 132.73, 130.97, 123.8, 120.8, 120.3, 114.3, 88.5; Mass Spectrum m/e (M+1) 223.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677383B1
Source datasetuspto-grants-2004_01
ORD IDord-e9a18e9930354cd18e8cd441ff4d9109
Source noteuspto-grants-2004_01