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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396333Generated: November 1, 2026

Ethoxalyl chloride → Ethyl [(3-chloro-2,6-difluorophenyl)carbamoyl]formate

https://huagongshe.com/reaction/1396333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxalyl chlorideHCID 20884—
Reactant3-Chloro-2,6-difluoroanilineHCID 17750745—
SolventTetrahydrofuranHCID 8028—
ProductEthyl [(3-chloro-2,6-difluorophenyl)carbamoyl]formateHCID 12351504372%

Reaction Steps

To a solution of 3-chloro-2,6-difluoroaniline (430 mg, 2.55 mmol) and TEA (0.5 mL, 3.59 mmol) in THF (5 mL) was added ethyl 2-chloro-2-oxoacetate (0.3 mL, 2.63 mmol). A white precipitate was formed immediately. After 30 min, the reaction mixture was filtered and rinsed with ether. The filtrate was concentrated to yield a crude yellow oil, which was purified by silica gel chromatography to yield the desired product (484 mg, 72%) as a white solid. 1H NMR (500 MHz, CDCl3) δ 8.42 (br. s., 1H), 7.35 (m, 1H), 6.98 (m, 1H), 4.45 (q, J=7.2 Hz, 2H), 1.45 (t, J=7.2 Hz, 3H). MS (ESI) m/z: 263.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901115B2
Source datasetuspto-grants-2014_12
ORD IDord-468de7c5843d466189b4ee58e640f275
Source noteuspto-grants-2014_12