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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094971Generated: October 31, 2026

Pyridine → HCID 23107570, compound

https://huagongshe.com/reaction/1094971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantVeratroyl chlorideHCID 77070—
ReactantMethyl 2-amino-5-bromobenzoateHCID 736224—
ProductHCID 23107570HCID 23107570—

Reaction Steps

Methyl 2-amino-5-bromobenzoate (compound A) (2.0 g) was dissolved in anhydrous methylene chloride (40.0 ml). Subsequently, pyridine (1.0 ml) and 3-(chloromethyl)benzoyl chloride (compound B) (2.0 g) were added to the solution at room temperature, and the mixture was stirred at that temperature for 3 hr. 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 5-bromo-2-[3-(chloromethyl)benzoyl]aminobenzoate as a useful intermediate (3.32 g, yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134015B2
Source datasetuspto-grants-2012_03
ORD IDord-5d25bbfcc2ba47f2b649f4b3bdba1b39
Source noteuspto-grants-2012_03