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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644013Generated: November 3, 2026

1,4-Cyclohexanedione → HCID 57805450, compound

https://huagongshe.com/reaction/1644013

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-CyclohexanedioneHCID 12511—
ReactantSodium HydroxideHCID 14798—
Reactant4,5-DifluorophthalaldehydeHCID 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 numberUS08119804B2
Source datasetuspto-grants-2012_02
ORD IDord-a4cac5d51f224868b5870a8bf20f1bfc
Source noteuspto-grants-2012_02