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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978164Generated: October 30, 2026

Phosphorus oxychloride → 4-Chloro-3-nitro-1,2-dihydropyridin-2-one

https://huagongshe.com/reaction/1978164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178526878HCID 178526878—
SolventTolueneHCID 1140—
Product4-Chloro-3-nitro-1,2-dihydropyridin-2-oneHCID 519282—

Reaction Conditions

Temperature47 °C

Reaction Steps

A 150 mL flask is charged with 2,4-dihydroxy-3-nitropyridine (Compound XII) (10.0 g, 0.064 mole), and toluene (30 mL). The mixture is stirred at moderate speed and warmed to 47° C. Phosphorus oxychloride (POCl3) (4.4 g, 0.0289 moles) is added over 10 minutes, via a syringe pump, giving an exotherm to 49° C. N,N-diisopropylethylamine (DIPEA )(2.22 g, 0.017 moles) is added over 10 minutes, giving an exotherm to 51° C. Another portion of POCl3 (4.4 g, 0.0289 moles) is added over 10 minutes, followed by another portion of DIPEA (2.22 g, 0.017 moles) over 10 minutes. A third portion of POCl3 (4.4 g, 0.0289 moles) is added over 10 minutes, followed by a third portion of DIPEA (2.22 g, 0.017 moles) over 10 minutes, followed by a final portion of POCl3 (4.4g, 0.0289 moles) over 10 minutes (total POCl3 added is 17.7 g), then by a final portion of DIPEA (2.22 g, 0.017 moles) over 10 min.(total DIPEA added is 8.9 g). The reaction is then stirred at 50° C. for 5 hr until IPC indicates complete consumption of Compound XII. The reaction is allowed to cool to 20° C. over 30 minutes and 50 mL of water is added over 1.5 hr allowing the temperature to rise to 47° C. This mixture is stirred for four hours while cooling to 25° C. The batch is filtered washing twice with 15 mL of water, then twice with 15 mL of toluene. The product is dried to give Compound II.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235909B1
Source datasetuspto-grants-2001_05
ORD IDord-e22a64082dfa4de38cf33039821d94e5
Source noteuspto-grants-2001_05