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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381926Generated: October 26, 2026

Phosphorus oxychloride → 2-(3-Chlorophenyl)-4-chloro-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone

https://huagongshe.com/reaction/381926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178504686HCID 178504686—
Product2-(3-Chlorophenyl)-4-chloro-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinoneHCID 2193437729%

Reaction Steps

A solution of 2-(3-chlorophenyl)-4-hydroxy-5-[4-(methylsulfonyl)phenyl]-3(2H)-pyridazinone, prepared in Example 332, in POCl3 was heated to reflux for 3 hours while stirring under nitrogen. The mixture was cooled to room temperature and poured into ice with constant swirling. The resulting white solid was extracted with ethyl acetate. The combined organics were washed with H2O, dried over MgSO4, and concentrated to a solid. The crude product was purified using flash chromatography (SiO2, eluting with 1:1 ethyl acetate/hexanes) to provide the desired product (yield: 0.151 g, 29%). mp 203-204° C. 1H NMR (300 MHz, DMSO d6) δ 3.29-3.36 (3H, obstructed by H2O), 7.60 (m, 3H), 7.76 (m, 1H), 7.92 (m, 2H), 8.14 (m, 2H), 8.25 (s, 1H). MS (DCI/NH3) m/z 395 (M+H)+, 412 (M+NH4)+. Anal. calc. for C17H12Cl2N2O3S: C, 51.66; H, 3.06; N, 7.09. Found: C, 51.67; H, 3.03; N, 6.93.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06307047B1
Source datasetuspto-grants-2001_10
ORD IDord-b67b562777ea42d1bb61af2c5db85363
Source noteuspto-grants-2001_10