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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171036Generated: November 2, 2026

4-Nitrobenzoyl chloride → 1-(4-Nitrophenyl)-1-propanone

https://huagongshe.com/reaction/1171036

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoyl chlorideHCID 8502—
ReactantHCID 178461633HCID 178461633—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Nitrophenyl)-1-propanoneHCID 9472640%

Reaction Steps

A solution of 0.5M ZnCl2 in THF (60 mL, 30 mmol) in THF (20 mL) at room temperature was treated with 2M ethyl magnesium chloride in THF (15 mL, 30 mmol) dropwise via syringe, cooled with an ice bath for about 10 minutes, stirred at room temperature for 20 minutes, cooled to 0° C., and treated sequentially with Pd(PPh3)4 (1.73 g, 1.5 mmol) and a solution of 4-nitrobenzoyl chloride (6.12 g, 33 mmol) in THF (20 mL). The mixture was stirred at 0° C. for 40 minutes, diluted with water and extracted three times with ethyl acetate. The combined extracts were washed with saturated Na2CO3, water, and brine, dried (MgSO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 6:1 hexanes/ethyl acetate to provide 2.17 g (40%) of the desired product. Rf=0.6 (3:1 hexanes/ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829570B2
Source datasetuspto-grants-2010_11
ORD IDord-314e5893ca454ed191fc01d7482381b3
Source noteuspto-grants-2010_11