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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251859Generated: November 2, 2026

Oxalyl chloride → Methyl 2-(chlorocarbonyl)-6-nitrobenzoate

https://huagongshe.com/reaction/2251859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-(Methoxycarbonyl)-3-nitrobenzoic acidHCID 243002—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(chlorocarbonyl)-6-nitrobenzoateHCID 12651086—

Reaction Steps

Oxalyl chloride (5.4 mL, 62.4 mmol) was added to a suspension of 3-nitro-phthalic acid 2-methyl ester (11.7 g, 52.0 mmol, Step A) in 150 mL of anhydrous CH2Cl2 at RT. A few drops of DMF were added, then the mixture was heated to reflux for 2 h, and cooled to RT. The mixture was washed with NaHCO3 (aq), brine, dried over MgSO4, filtered, and condensed to give the titled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320992B2
Source datasetuspto-grants-2008_01
ORD IDord-e28e563902e84b93bd7311a1fd4c2b57
Source noteuspto-grants-2008_01