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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569990Generated: October 30, 2026

1-Ethylpiperidine-2,4-dione → 1-Ethyl-3-methoxymethylenepiperidine-2,4-dione

https://huagongshe.com/reaction/569990

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethylpiperidine-2,4-dioneHCID 13784119—
ReactantMethylorthoformateHCID 53629101—
SolventAcetic AnhydrideHCID 7918—
Product1-Ethyl-3-methoxymethylenepiperidine-2,4-dioneHCID 5409215225.1%

Reaction Steps

Added to 8.3 g of 1-ethylpiperidine-2,4-dione were 11 g of methyl orthoformate and 20 ml of acetic anhydride. The resultant mixture was refluxed for 7 hours. After allowing the reaction mixture to cool down, excess methyl orthoformate and acetic anydride were distilled off under reduced pressure. The brown residue was distilled under reduced pressure in a Kugelroll apparatus (0.5 mmHg; bath temperature: 200°-250° C.) to obtain 2.7 g of 1-ethyl-3-methoxymethylenepiperidine-2,4-dione as crystals (yield: 25%). The crystals were recrystallized from a mixed solvent of ethyl acetate and hexane to obtain needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04734418
Source datasetuspto-grants-1988_03
ORD IDord-31eebf9e4afb46a98abce0f961ffe098
Source noteuspto-grants-1988_03