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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109366Generated: October 29, 2026

Triethylamine → HCID 53762281, compound

https://huagongshe.com/reaction/1109366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
Reactant4-Hydroxy-3,5-bis(isopropyl)benzaldehydeHCID 82712—
ReactantHCID 19022168HCID 19022168—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 53762281HCID 5376228145.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 5.90 g (6 mmol) of (1-acetyl-2-oxopyrrolidin-3-yl)triphenylphosphonium bromide in ethanol (12 ml) were added 1.24 g (6 mmol) of 3,5-di-isopropyl-4-hydroxybenzaldehyde and 1.67 ml (12 mmol) of triethylamine, and the mixture was stirred with heating at 60° C. for 2 hours. The reaction mixture was evaporated to give a residue, which was added with ethyl acetate and water. The ethyl acetate layer was washed with water, dried over magnesium sulfate and evaporated to give a residue, which was chromatographed on silica gel (toluene/ethyl acetate=4/1) to give 857 mg of the objective compound in 45% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05319099
Source datasetuspto-grants-1994_06
ORD IDord-3f1f9a16b884455a8bd41d2986af3827
Source noteuspto-grants-1994_06