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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130912Generated: November 2, 2026

Acetic Acid → HCID 68747527, compound

https://huagongshe.com/reaction/130912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantNitromethaneHCID 6375—
Reactant3-Chloro-4-hydroxybenzaldehydeHCID 17022—
ReactantAmmonium AcetateHCID 517165—
ProductHCID 68747527HCID 6874752780%

Reaction Conditions

Temperature110 °C

Reaction Steps

The 3-chloro-4-hydroxy-benzaldehyde (980 mg, 6.3 mmol), nitromethane (2.0 mL, 37.7 mmol) and ammonium acetate (1.9 g, 25.1 mmol) were dissolved in acetic acid (9 mL) and the reaction heated at 110° C. for 2 hours. The reaction is concentrated under reduced pressure and the residue partitioned between ether and water. Separate the layers and dry with Na2SO4, filter and concentrate under reduced pressure. Purify the crude product by flash chromatography (eluent: EtOAc/hexane 20/80 and 30/70) afforded the title compound (1.0 g, 80%). 1H-NMR (CDCl3, 200 MHz): 8.34 (d, 1H, J=13.4 Hz), 7.82 (d, 1H, J=13.4 Hz), 7.71 (d, 1H, J=8.6 Hz), 6.94 (d, 1H, J=2.4 Hz), 6.80 (dd, 1H, J=2.4 and 8.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381719B2
Source datasetuspto-grants-2008_06
ORD IDord-3ec4e1d8c9004172be6b870fc49a340e
Source noteuspto-grants-2008_06