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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879120Generated: November 2, 2026

Triethylamine → HCID 59760055, compound

https://huagongshe.com/reaction/1879120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactantp-Aminophenylacetic acid ethyl esterHCID 225219—
Reactant6-Chloro-2-fluoro-3-methoxybenzoic acidHCID 3856039—
CatalystDimethylformamideHCID 6228—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59760055HCID 5976005594.1%

Reaction Steps

Oxalyl chloride (193 μl, 2.21 mmol) was added dropwise to a solution of 6-chloro-2-fluoro-3-(methyloxy)benzoic acid (300 mg, 1.47 mmol) in dichloromethane (5 ml). To this was added dimethylformamide (1 drop) and the reaction was stirred at room temperature for 3 hrs. The solvent was evaporated to afford a yellow semi-solid. This semi-solid was dissolved in dichloromethane (5 ml) and ethyl (4-aminophenyl)acetate (316 mg, 1.76 mmol) followed by triethylamine (287 μl, 2.06 mmol) were added. The resultant solution was stirred at room temperature overnight. The reaction was diluted with water and the phases separated. The organic layer was dried (Na2SO4), the solvent evaporated and the residue purified by flash chromatography (Biotage SP4, 25+M silica column, 0→50% ethyl acetate/petrol) to afford the title as a yellow semi-solid (506 mg, 94%). MS (ES+) m/z 366 [M+H+] (C18H1735ClFNO4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314147B2
Source datasetuspto-grants-2012_11
ORD IDord-25cb468d47474fd88cd11393199e1a9a
Source noteuspto-grants-2012_11