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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286125Generated: November 1, 2026

Ethanol → HCID 12832890, compound

https://huagongshe.com/reaction/2286125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDiethyl OxalateHCID 7268—
ReactantSodium hydrideHCID 24758—
Reactant1-(2,3-Dichlorophenyl)ethan-1-oneHCID 91986—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 12832890HCID 1283289034.4%

Reaction Steps

To 14 g of sodium hydride (50%) were added dropwise 21.3 g of diethyl oxalate, 0.54 ml of ethanol and then 160 ml of ether solution containing 30 g of 2,3-dichloroacetophenone with stirring under cooling with ice. The reaction was carried out under the state free from water. The reaction was continued at room temperature for 40 minutes with stirring after the dropping and further carried out for 45 minutes under reflux. The reaction mixture was poured into ice-cold water containing 17.5 g of acetic acid and after stirring the mixture was filtered. The organic layer was separated, dehydrated and concentrated. The residue was recrystallized from n-hexane to obtain 14.5 g of ethyl 4-(2,3-dichlorophenyl)-2,4-dioxobutyrate (white needles, m.p. 57°-58° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04326881
Source datasetuspto-grants-1982_04
ORD IDord-efc0a605937e42e28324492bd234ace1
Source noteuspto-grants-1982_04