Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886120Generated: November 3, 2026

(4-Nitrophenyl)acetic acid → 2-(4-nitrophenyl)-1-phenylethanone

https://huagongshe.com/reaction/1886120

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Nitrophenyl)acetic acidHCID 4661—
ReactantOxalyl chlorideHCID 65578—
SolventBenzeneHCID 241—
Product2-(4-nitrophenyl)-1-phenylethanoneHCID 234510—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-nitrophenylacetic acid (200 g) in benzene (1.5 L) was added oxalyl chloride (200 mL). The mixture was warmed to 50°-60° C. for 2 hrs, after which time benzene and excess oxalyl chloride were distilled off under vacuum at 50° C. until a final volume of 500 mL was achieved. The residue was diluted with benzene (1 L) and cooled to 0° C. To this was added anhydrous aluminum chloride (160 g) portion-wise over 15 minutes. Thereafter, the mixture was stirred overnight at room temperature. The reaction mixture was poured over a mixture of ice (3 L) and concentrated HCl (1 L). The resulting slurry was filtered through celite and the precipitate washed with ethyl acetate. The combined filtrates were washed with water, saturated sodium bicarbonate and with brine, dried over sodium sulfate and evaporated to give 227 grams of 2-(4-nitrophenyl)-1-phenylethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05149709
Source datasetuspto-grants-1992_09
ORD IDord-de046a3dc61842c9974c8cf285dfda5e
Source noteuspto-grants-1992_09