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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588662Generated: October 30, 2026

Oxalyl chloride → HCID 89498529, compound

https://huagongshe.com/reaction/588662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 89498250HCID 89498250—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 89498529HCID 89498529—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of EXAMPLE 23C (7.89 g) in DMF (80 mL) and pyridine (5 mL) at 0° C. was added dropwise oxalyl chloride (5.52 mL). The mixture was stirred at 0° C. for 30 minutes and ice-water was added to quench the reaction. The resulting mixture was diluted with ethyl acetate and washed with aqueous NaHCO3 and water extensively. The organic layer was dried over Na2SO4, filtered, and concentrated. The residue was purified by flash column, eluting with dichloromethane to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227963B2
Source datasetuspto-grants-2016_01
ORD IDord-cc483ffe34c84f489478107316fc567f
Source noteuspto-grants-2016_01