Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500105Generated: October 31, 2026

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

https://huagongshe.com/reaction/500105

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 numberUS07767675B2
Source datasetuspto-grants-2010_08
ORD IDord-e45c337d8e93451f8c8916c24918d5d7
Source noteuspto-grants-2010_08