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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244649Generated: October 31, 2026

Methyl Ethyl Ketone → HCID 178468923, compound

https://huagongshe.com/reaction/244649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantDiethyl OxalateHCID 7268—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium ethoxideHCID 2723922—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 178468923HCID 178468923—

Reaction Steps

To a solution of diethyl ethanedioate (45.2 g) in absolute ethanol (140 ml) cooled in an ice/industrial methylated spirit bath was added ethanolic sodium ethoxide (100 ml; 21% w/w) dropwise, keeping the temperature below 3° C. and the mixture stirred for 15 min in an ice bath. 2-Butanone (22.1 g) was added and the mixture stirred in an ice bath for 15 min before being allowed to warm to RT overnight. The mixture was stirred at 40° C. for 6 h and then cooled to 0° C. Glacial acetic acid (17.5 ml) was added dropwise, maintaining the temperature below 3° C. The resultant precipitate was broken up and ethanol (100 ml) added to enable the mixture to stir. Hydrazine hydrate (14 ml) was added dropwise, maintaining the temperature below 7° C. The mixture was stirred in the cold bath for 10 min and then allowed to warm to RT overnight. The solvent was removed in vacuo and the residue partitioned between DCM (300 ml) and water (100 ml). The organic phase was washed with water (2×100 ml), dried over magnesium sulphate and the solvent removed to give the title compound (41.3 g) as a red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658635B2
Source datasetuspto-grants-2014_02
ORD IDord-6fadb195428b4c7cb109489293fcf129
Source noteuspto-grants-2014_02