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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964617Generated: October 25, 2026

4'-Hydroxyacetophenone → 4-Hydroxy-3-Nitroacetophenone

https://huagongshe.com/reaction/964617

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-HydroxyacetophenoneHCID 7469—
ReactantPotassium NitrateHCID 24434—
CatalystPotassium NitrateHCID 24434—
SolventSulfuric AcidHCID 1118—
Product4-Hydroxy-3-NitroacetophenoneHCID 13872394.7%

Reaction Steps

To mechanically stirred conc. H2SO4 (700 mL) at 3° C. was added p-hydroxyacetophenone (66.0 g, 480 mmol) followed by KNO3 (48.3 g, 477 mmol) in two approximately equal portions about four minutes apart. An additional 3.76 g of KNO3 was added after 1.67 hours to insure reaction completion. The reaction was slowly poured into 8 L crushed ice/water and extracted with 4 L ethyl acetate (EtOAc). The extract was concentrated in vacuo to a volume of ~1.25 L, 500 mL heptane were added and concentration was continued. Once a thick yellow suspension formed at 50° C., it was cooled to ~10° C. and filtered. The collected solids were washed with ~150 mL heptane and dried in vacuo at ~40° C. to give 81.8 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05770615
Source datasetuspto-grants-1998_06
ORD IDord-1b9405fe1d3b454593f3511a1cfa4c43
Source noteuspto-grants-1998_06