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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094970Generated: November 1, 2026

Pyridine → HCID 835412, compound

https://huagongshe.com/reaction/1094970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl AnthranilateHCID 8635—
ReactantVeratroyl chlorideHCID 77070—
SolventDichloromethaneHCID 6344—
ProductHCID 835412HCID 835412—

Reaction Steps

Methyl 2-aminobenzoate (compound A) (2.0 g) was dissolved in anhydrous methylene chloride (40.0 ml). Subsequently, pyridine (2.0 ml) and 3,4-dimethoxybenzoyl chloride (compound B) (3.14 g) were added to the solution at room temperature, and the mixture was stirred at that temperature for 30 min. After the completion of the reaction, distilled water was added thereto, and the mixture was subjected to separatory extraction with chloroform. The organic layer was washed with a saturated aqueous sodium chloride solution, was dried over sodium sulfate, and was then concentrated to give methyl 2-[(3,4-dimethoxybenzoyl)amino]benzoate as a useful intermediate (4.17 g, yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134015B2
Source datasetuspto-grants-2012_03
ORD IDord-33bbed43589b47e78e85dc326d039089
Source noteuspto-grants-2012_03