Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519401Generated: November 3, 2026

Acetaldehyde → 2-Ethylcyclohexane-1,3-dione

https://huagongshe.com/reaction/1519401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantPyridineHCID 1049—
Reactant1,3-CyclohexanedioneHCID 10434—
ReactantHantzsch esterHCID 70849—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2-Ethylcyclohexane-1,3-dioneHCID 1089880569%

Reaction Steps

1,3-Cyclohexanedione (10 g, 89.2 mmol), 40% aqueous CH3CHO (49.4 g, 445.9 mmol) were dissolved in methanol (40 mL) followed by addition of Hantzsch ester (22.7 g, 89.2 mmol) and pyridine (2.1 g, 18.74 mmol) under nitrogen. The resulting light yellow mixture was stirred at room temperature overnight, then concentrated to give crude product that was re-slurried in a mixture of CH2Cl2 (40 mL) and hexanes (60 mL) to furnish 2-ethyl-1,3-cyclohexanedione (8.6 g, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073888B2
Source datasetuspto-grants-2015_07
ORD IDord-0be1b85333fe4f2e857f2598abcd2658
Source noteuspto-grants-2015_07