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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium 2-((2,6-dichloro-3-methylphenyl)amino)benzoate | HCID 4038 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzoic acid, 2-((2,6-dichloro-3-methylphenyl)amino)-, methyl ester | HCID 76743 | 70.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05462952 |
|---|
| Source dataset | uspto-grants-1995_10 |
|---|
| ORD ID | ord-88922598cb3543b5a30c2ca64c9ece3d |
|---|
| Source note | uspto-grants-1995_10 |
|---|