Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729171Generated: November 1, 2026

Diethyl Oxalate → HCID 14871092, compound

https://huagongshe.com/reaction/729171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl OxalateHCID 7268—
ReactantP-ChloroacetophenoneHCID 7467—
Reactant1,3-Diphenyl-1H-pyrazoleHCID 613284—
Reactant4-Methoxyphenylhydrazine hydrochlorideHCID 2723904—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 67830464HCID 67830464—
SolventEthanolHCID 702—
ProductHCID 14871092HCID 14871092—

Reaction Steps

Ethyl 4-(4-chlorophenyl)-2,4-dioxobutanoate sodium salt (10.0 g, 36.1 mM), synthesized from 4-chloroacetophenone and diethyloxalate employing lithiumdiisopropylamide as base, and 4-methoxyphenylhydrazine hydrochloride (6.31 g, 36.1 mM) in cold absolute EtOH (360 ml) were stirred at 0° for 4hr., at rt for 18 hr and then at reflux for 5 hr. The resulting solution was evaporated in vacuo, H2O (100 ml) was added and the aqueous phase extracted with Et2O (3×100 ml). The combined ether layerwas washed (brine), dried (Na2SO4) and concentrated in vacuo to give a crude solid which by NMR was a 5:1 mixture of the title compound tothe corresponding 1,3-diphenyl pyrazole. Recrystallization from EtOAc:hexane (2×) afforded pure 1 (7.93 g, 61%) as a white solid, mp=107°-108° C., MS, (DCI) m/e 357 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05051518
Source datasetuspto-grants-1991_09
ORD IDord-529e242da2de486dbac2e1d29a04d345
Source noteuspto-grants-1991_09