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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104939Generated: October 29, 2026

1,4-Cyclohexanedione → HCID 57805450, compound

https://huagongshe.com/reaction/2104939

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-CyclohexanedioneHCID 12511—
ReactantSodium HydroxideHCID 14798—
Reactant4,5-Difluoro-1,2-benzenedicarboxaldehydeHCID 22628907—
SolventEthanolHCID 702—
ProductHCID 57805450HCID 5780545065.7%

Reaction Steps

To a solution of 4,5-difluorophthalaldehyde (Compound 22)(0.48 g, 2.8 mmol, 2 molar equivalents) and 1,4-cyclohexanedione (0.16 g, 1.4 mmol, 1 molar equivalent) in ethanol (40 ml) was added a solution of 5% aqueous NaOH (0.6 ml) at room temperature. The reaction mixture was stirred for 30 minutes at room temperature and then warmed to 60° C. After 1 hour at 60° C., the reaction mixture was cooled to room temperature. The resulting precipitate was filtered, washed with water (15 ml), ethanol (30 ml) and diethyl ether (30 ml) to give the title compound as a yellow powder (0.35 g, 64%) used as obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576208B2
Source datasetuspto-grants-2009_08
ORD IDord-309e2277b6294e41b8a563b0496216d1
Source noteuspto-grants-2009_08