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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462818Generated: October 25, 2026

Phosphorus oxychloride → 2,3-Dichloro-5-iodopyridine

https://huagongshe.com/reaction/462818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantHCID 178517798HCID 178517798—
SolventDichloromethaneHCID 6344—
Product2,3-Dichloro-5-iodopyridineHCID 2189287464%

Reaction Conditions

Temperature130 °C

Reaction Steps

A 100 ml 3-necked round bottom flask, fitted with a condenser topped with a N2 inlet, a mechanical stirrer and a thermometer, was charged with 17.2 g (0.0673 mole) of 3-chloro-2-hydroxy-5-iodopyridine, 14.85 g (0.0713 mole) of PCl5, and 1 ml (1.68 g; 0.0109 mole) of POCl3. The reaction mixture, containing solids, was slowly stirred and slowly heated to 130° C. The reaction mixture was stirred under N2 for 5 hours after which it was cooled to room temperature and allowed to stand overnight. The reaction mixture was cautiously poured into crushed ice and allowed to stand for 1 hour. Methylene chloride (200 ml) was added to the reaction mixture to dissolve the solids present in it. The layers was separated and the organic phase was washed with dilute base, water and saturated NaCl. After drying over anhydrous MgSO4 and filtration, the solvent was evaporated leaving 11.8 g of a yellow solid. The solid was recrystallized from methanol resulting in 6.60 g of solid that had spectral and physical properties identical to the product obtained in Example 1, STEP D.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04517368
Source datasetuspto-grants-1985_05
ORD IDord-082aafd763bd47a08e2e03f7ceada57f
Source noteuspto-grants-1985_05