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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251860Generated: November 2, 2026

Methyl 2-(chlorocarbonyl)-6-nitrobenzoate → Methyl 2-acetyl-6-nitrobenzoate

https://huagongshe.com/reaction/2251860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-(chlorocarbonyl)-6-nitrobenzoateHCID 12651086—
ReactantHCID 178418546HCID 178418546—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-acetyl-6-nitrobenzoateHCID 59644399—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a suspension of copper(I)cyanide (5.70 g, 63.6 mmol) in 200 mL of anhydrous THF at −78° C. was added methyl magnesium bromide (1.4 M in toluene and THF, 43 mL, 59.3 mmol). The mixture was stirred at −20° C. for 20 min, then cooled to −78° C. A solution of 2-chlorocarbonyl-6-nitro-benzoic acid methyl ester (11.6 g, 47.8 mmol, Step B) in 30 mL of THF was added. The mixture was cooled at −10° C., and slowly warmed to RT, quenched with NH4Cl(aq), and extracted with EtOAc. The combined organic portions were washed with brine, dried over MgSO4, filtered, condensed, and purified by flash column chromatography, to provide the titled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320992B2
Source datasetuspto-grants-2008_01
ORD IDord-673a74252478423db9562632fdee041b
Source noteuspto-grants-2008_01