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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257765Generated: November 3, 2026

Phosphorus oxychloride → 3-Chloro-6-(4-fluorophenyl)-1,2,4-triazine

https://huagongshe.com/reaction/1257765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant6-(4-Fluorophenyl)-1,2,4-triazin-3(2H)-oneHCID 12581284—
SolventChloroformHCID 6212—
Product3-Chloro-6-(4-fluorophenyl)-1,2,4-triazineHCID 21315219—

Reaction Steps

A mixture of 6-(4-fluorophenyl)-1,2,4-triazin-3(2H)-one (1.0 g, 5.23 mmol) and phosphoryl chloride (8.0 mL) in chloroform (5.0 mL) was heated under reflux conditions overnight. After cooling, the volatiles were removed under reduced pressure. The residue was dissolved in dichloromethane (60 mL) and was poured into ice with stirring. The mixture was neutralized with aqueous 2N potassium carbonate and filtered through a pad of Celite. The organic layer was separated and the aqueous layer was extracted with dichloromethane (3×20 mL). The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography to give the desired product. (600 mg, 54.6%) 1H-NMR (300 MHz, CDCl3): 8.88 (s, 1H), 8.06-8.12 (m, 2H), 7.06-7.14 (m, 2H). LCMS: (M+H)=210.1/212.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461330B2
Source datasetuspto-grants-2013_06
ORD IDord-41c44009e0234d038008db95a390e716
Source noteuspto-grants-2013_06