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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227446Generated: October 30, 2026

Triethylamine → HCID 131723365, compound

https://huagongshe.com/reaction/2227446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydrazine, (4-chlorophenyl)-, hydrochloride (1:1)HCID 71600—
Reactant3,5-Dichloropyridine-4-carbon chlorideHCID 11572022—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131723365HCID 13172336596%

Reaction Steps

Triethylamine (1.40 mL, 1.02 g, 10.1 mmol) was added to a suspension of 4-chlorophenylhydrazine hydrochloride (1.83 g, 98%, 10.0 mmol) in THF (75 mL). The mixture was stirred under nitrogen at room temperature for 2.75 h. More triethylamine (3.0 mL, 21.6 mmol) was added followed by dropwise addition of a solution of freshly-prepared 3,5-dichloropyridine-4-carbonyl chloride (10.0 mmol) in THF (20 mL). After stirring overnight, the reaction mixture was concentrated under reduced pressure. The residue was partitioned between ethyl acetate (100 mL) and water (50 mL). The layers were shaken together and allowed to separate. The organic phase was dried (Na2SO4) and concentrated, leaving 3.04 g of a tan solid, mp 201-203.5° C. Recrystallized from ethyl acetate/cyclohexane and then from ethanol furnished crystals which melted at 206-207.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413992B1
Source datasetuspto-grants-2002_07
ORD IDord-68c9ac8f2fc04ff8b29cbf5e4548d782
Source noteuspto-grants-2002_07