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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451061Generated: November 1, 2026

Pyridine → HCID 727211, compound

https://huagongshe.com/reaction/1451061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl chloroformateHCID 6586—
ReactantMethyl 4-aminobenzoateHCID 12082—
Reactant2-DimethylaminopyridineHCID 21885—
SolventDichloromethaneHCID 6344—
ProductHCID 727211HCID 72721171.7%

Reaction Steps

Methyl 4-aminobenzoate (Aldrich, 5.0 g, 33 mmol) was dissolved in 120 mL of anhydrous methylene chloride containing pyridine (3.2 mL, 39.6 mmol) and dimethylaminopyridine (DMAP, 500 mg) was added. To the ice-cooled mixture was added methyl chloroformate (2.80 mL, 36.3 mmol) while stirring. The stirring was continued for 16 h at room temperature. The reaction was quenched with water (50 mL) and the organic layer separated. The aqueous layer was extracted with chloroform (50 mL). The combined organic extract was dried over sodium sulfate. The volatiles were evaporated on a rotoevaporator to give a residue, which was crystallized from chloroform-methanol. The white solid was separated, dried in air followed by drying in a pistol at acetone reflux in vacuo to give 4.95 g (71.7%) of methyl 4-(methoxycarbonyl)aminobenzoate, mp 177°-178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602277
Source datasetuspto-grants-1997_02
ORD IDord-09e2094410004b7185b491e4b00df360
Source noteuspto-grants-1997_02