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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211166Generated: October 30, 2026

Methanol → Benzoic acid, 2-((2,6-dichloro-3-methylphenyl)amino)-, methyl ester

https://huagongshe.com/reaction/2211166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium 2-((2,6-dichloro-3-methylphenyl)amino)benzoateHCID 4038—
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
SolventDichloromethaneHCID 6344—
ProductBenzoic acid, 2-((2,6-dichloro-3-methylphenyl)amino)-, methyl esterHCID 7674370.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Oxalyl chloride (9.50 g, 74.8 mmol) in 20 ml of methylene chloride is added dropwise to a 0° C. suspension of meclomen (10.20 g, 34.4 mmol) and dimethylformamide (2.70 ml, 34.7 mmol) in 50 ml of methylene chloride. The clear yellow solution is stirred at 0° C. for 90 minutes then added by cannula to 110 ml of methanol at room temperature. The white suspension is stirred at room temperature overnight. The white solid is collected providing 7.52 g of product. The filtrate is concentrated and the residue partitioned between ethyl acetate and water. The organic layer is washed with brine, dried over magnesium sulfate and concentrated, providing an additional 2.45 g of product (94% total), mp 130°-131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05462952
Source datasetuspto-grants-1995_10
ORD IDord-88922598cb3543b5a30c2ca64c9ece3d
Source noteuspto-grants-1995_10