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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879116Generated: November 1, 2026

Acetic Acid → HCID 59163334, compound

https://huagongshe.com/reaction/1879116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 59163380HCID 59163380—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
ProductHCID 59163334HCID 5916333485.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of ethyl (4-{[(2-chloro-5-nitrophenyl)carbonyl]amino}phenyl)acetate (2.27 g, 6.3 mmol) in EtOH (20 ml) was heated at 50° C. A 20% aqueous solution of acetic acid (10 ml) was added followed by iron (6 eq, 37.6 mmol, 2.1 g). The mixture was heated at 80° C. for 30 minutes. On cooling the mixture was filtered through celite washing with EtOH. Solvent evaporated in vacuo. Residue taken up in EtOAc and aqueous sodium bicarbonate. Layers separated, aqueous layer extracted with EtOAc (×2). Organic layers combined and washed with brine, dried over magnesium sulphate and evaporated. The residue was purified by column chromatography (Biotage SP4, 100 g silica column) eluting with 25-75% ethyl acetate in hexanes to afford the title compound as a light yellow oil (1.8 g). MS (ES+) m/z 333 [M+H]+ (C17H1735ClN2O3). 1H-NMR (400 MHz, d6-DMSO) δ 1.18 (3H, m), 3.61 (2H, s), 4.05 (2H, m), 5.47 (2H, s), 6.65 (2H, m), 7.12 (1H, d, J 8.4), 7.22 (2H, d, J 8.4), 7.64 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314147B2
Source datasetuspto-grants-2012_11
ORD IDord-b4625a05f04e4d94944dc6273c945e0c
Source noteuspto-grants-2012_11