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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708856Generated: October 29, 2026

Pyridine → HCID 178460113, compound

https://huagongshe.com/reaction/1708856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantNitrobenzeneHCID 7416—
ReactantAcryloyl chlorideHCID 13140—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178509129HCID 178509129—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178460113HCID 17846011332.1%

Reaction Steps

Next, 17 g (0.05 mol) of the 3-amino-1-(2,4,6-trichlorophenyl)-4-pyrazolyl-5-oxo-2-pyrazoline was dissolved in 300 ml qf tetrahydrofuran, to which were added 10 ml (0.13 mol) of pyridine and 1 ml of nitrobenzene. Then, 31.1 g (0.12 mol) of acrylic acid chloride was added under cooling with ice, after which the mixture was stirred for 1.5 hours. Next, 500 ml of water was added, extraction with ethyl acetate was effected, and the extract was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, the residual oil was dissolved in 150 ml of ethanol, and then 60 ml of water containing 3.0 g (0.074 mol) of sodium hydroxide was added at room temperature. After being stirred for 30 min, 3 ml of acetic acid was added to neutralize the solution, the separated oil was extracted with ethyl acetate, the extract was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residual oil was purified by silica gel column chromatography to yield 6.4 g (32%) of the title compound. Melting point: 151° to 154° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04946771
Source datasetuspto-grants-1990_08
ORD IDord-1892666bcfea46f497961e37982ce875
Source noteuspto-grants-1990_08