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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677070Generated: November 1, 2026

Pyridine → HCID 67378613, compound

https://huagongshe.com/reaction/1677070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 67371742HCID 67371742—
SolventWaterHCID 962—
ProductHCID 67378613HCID 67378613—

Reaction Steps

Under ice-cooling, oxalyl chloride (392 μL) was added dropwise into a dichloromethane (4 mL) solution containing (S)-1-[(2R,5S)-5-(4-fluorophenyl)pyrrolidine-2-yl]ethanol (479 mg) and pyridine (1 mL). Stirring was continued for 1 hour at the same temperature and for 1 hour at room temperature. Water was added, and the organic layer was partitioned, and the resultant was dried over anhydrous magnesium sulfate. The solvent was removed under a vacuum, and the residue was purified by silica gel column chromatography (heptane/ethyl acetate→ethyl acetate), and the title compound (130 mg) was obtained. The physical property values are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008293B2
Source datasetuspto-grants-2011_08
ORD IDord-4df4a0576e1944bd84389e93cd05d5ff
Source noteuspto-grants-2011_08