Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512708Generated: October 27, 2026

Sodium Chloride → 3-Chloro-1-(pyridine-3-yl)-4,5-dihydro-1H-pyrazole-5-carbonitrile

https://huagongshe.com/reaction/512708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantAcrylonitrileHCID 7855—
ReactantChlorosuccinimideHCID 31398—
ReactantPotassium BicarbonateHCID 516893—
Reactant(2E)-2-(pyridin-3-ylhydrazinylidene)acetic acid;hydrochlorideHCID 118022438—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product3-Chloro-1-(pyridine-3-yl)-4,5-dihydro-1H-pyrazole-5-carbonitrileHCID 11802277171.9%

Reaction Steps

(E)-2-((2-Pyridin-3-yl)hydrazono)acetic acid hydrochloride (2.00 g, 9.42 mmol) was stirred in ethyl acetate (47.1 mL). N-Chlorosuccinimide (2.36 g, 19.3 mmol), acrylonitrile (1.85 mL, 28.3 mmol) and potassium bicarbonate (2.86 g, 28.3 mmol) were added. Water (0.05 mL) was added and the mixture was stirred at room temperature for 18 hours. Saturated aqueous sodium chloride (brine, 50 mL) was added and the mixture was filtered through Celite®. The filter cake was washed with ethyl acetate (40 mL) and the layers were separated. The organic layers were combined, dried and concentrated to afford a residue. The resulting residue was purified by flash column chromatography using 80-100% ethyl acetate/hexanes as eluent to afford the desired product as an orange solid (1.40 g, 57.5%): 1H NMR (400 MHz, CDCl3) δ 8.51 (dd, J=2.9, 0.7 Hz, 1H), 8.33 (dd, J=4.7, 1.4 Hz, 1H), 7.51 (ddd, J=8.4, 2.9, 1.4 Hz, 1H), 7.30 (ddd, J=8.5, 4.7, 0.8 Hz, 1H), 5.06 (dd, J=11.3, 5.9 Hz, 1H), 3.64 (dd, J=17.4, 11.3 Hz, 1H), 3.51 (dd, J=17.4, 5.9 Hz, 1H); 13C NMR (101 MHz, CDCl3) δ 143.34, 142.79, 140.11, 136.16, 123.92, 121.93, 115.80, 51.39, 43.04; ESIMS m/z 207 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102654B2
Source datasetuspto-grants-2015_08
ORD IDord-ad3a4e96e5d64bdbb6f9dce2dac00920
Source noteuspto-grants-2015_08