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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166270Generated: November 1, 2026

Oxalyl chloride → Methyl 3-methyl-2-phenylquinoline-4-carboxylate

https://huagongshe.com/reaction/1166270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-Methyl-2-phenylquinoline-4-carboxylic acidHCID 673710—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-methyl-2-phenylquinoline-4-carboxylateHCID 230804100%

Reaction Steps

30 g (114 mmol) of 3-methyl-2-phenylquinoline-4-carboxylic acid (CAS [43071-45-0]) were suspended in 250 ml of dry CH2Cl2; 20 ml (230 mmol) of oxalyl chloride dissolved in 120 ml of CH2Cl2 were added dropwise and the reaction mixture was stirred at room temperature for 30 min. Two drops of DMF were added and the reaction was stirred for additional 30 min. The solvent was evaporated in vacuo to dryness, the residue was taken up with 100 ml of CH2Cl2 and 100 ml of MeOH, dissolved in 400 ml of CH2Cl2, were added dropwise. After stirring for 18 h the solvent was evaporated in vacuo to dryness, the residue was taken up with CH2Cl2 and washed with 1% NaHCO3; the organic layer was dried over anhydrous Na2SO4, filtered and evaporated in vacuo to dryness to yield 31.6 g of the title compound as a solid, which was used in the following reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613770B1
Source datasetuspto-grants-2003_09
ORD IDord-5655313579d74ca19616e6049c2fa73b
Source noteuspto-grants-2003_09