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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895821Generated: October 28, 2026

Acetic Acid → HCID 178468923, compound

https://huagongshe.com/reaction/895821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantDiethyl OxalateHCID 7268—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductHCID 178468923HCID 17846892389.2%

Reaction Steps

Ethanolic sodium ethoxide solution (21% w/w; 143 ml, 0.39 mol) was added dropwise to a stirred, ice-cooled solution of diethyl oxalate (59.8 ml, 0.44 mol) in absolute ethanol (200 ml) under nitrogen and the resulting solution stirred for 15 minutes. Butan-2-one (39 ml, 0.44 mol) was then added dropwise, the cooling bath removed, the reaction mixture stirred for 18 hours at room temperature and then for 6 hours at 40° C., then the cooling bath reintroduced. Next, glacial acetic acid (25 ml, 0.44 mol) was added dropwise, the resulting solution stirred for 30 minutes at 0° C., hydrazine hydrate (20 ml, 0.44 mol) added dropwise, then the reaction mixture allowed to warm to room temperature and maintained there over a period of 18 hours, before being evaporated under reduced pressure. The residue was partitioned between dichloromethane (300 ml) and water (100 ml), then the organic phase separated, washed with water (2×100 ml), dried (Na2SO4) and concentrated under reduced pressure to give the title compound (66.0 g). δ (CDCl3): 1.04 (3H, t), 1.16 (3H, t), 2.70 (2H, q), 4.36 (2H, q), 6.60 (1H, s). LRMS: m/z 169 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916927B2
Source datasetuspto-grants-2005_07
ORD IDord-91ba6b5f1b4140b1a39830bc9e144785
Source noteuspto-grants-2005_07