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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274594Generated: October 31, 2026

Ethyl 2,4-dioxovalerate → HCID 89649760, compound

https://huagongshe.com/reaction/2274594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2,4-dioxovalerateHCID 69208—
ReactantHCID 53418411HCID 53418411—
SolventAcetic AcidHCID 176—
ProductHCID 89649760HCID 89649760100.4%

Reaction Steps

To a solution of 5-bromo-2-hydrazinylbenzoic acid hydrochloride (60.0 g, 225.6 mmol) in AcOH (600 mL) was added ethyl-2,4-dioxovalerate (35.67 g, 225.6 mmol) followed by refluxing for 3 h. AcOH was evaporated invacuo and the residue was co-distilled with toluene (100 mL), twice. The residue was dissolved in EtOAc and washed with water until the aq. layer became neutral. The organic layer was dried over sodium sulphate and concentrated invacuo. The gummy material was triturated with diethyl ether to afford the title compound as a brown colored oil 80 g (100%), which was used without further purification for the next step. Rf=0.23 (10% MeOH in DCM); 1H NMR (400 MHz, DMSO-d6): δ 13.80-12.80 (brs, 1H), 8.08 (d, J=1.9 Hz, 1H), 7.96 (dd, J=2.4&8.3 Hz, 1H), 7.53 (d, J=8.3 Hz, 1H), 6.70 (s, 1H), 4.26 (q, J=7.2 Hz, 2H), 2.13 (s, 3H), 1.28 (t, J=7.1 Hz, 3H); ES-MS: m/z 353.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126979B2
Source datasetuspto-grants-2015_09
ORD IDord-7837310ed4ce4654900b3bc97213f683
Source noteuspto-grants-2015_09