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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726338Generated: October 30, 2026

Pyridine → HCID 19710732, compound

https://huagongshe.com/reaction/726338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl 4-oxocyclohexanecarboxylateHCID 317638—
Reactant(4-(Benzyloxy)phenyl)hydrazine monohydrochlorideHCID 3016725—
SolventEthanolHCID 702—
ProductHCID 19710732HCID 1971073285.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of 3.242 gm (12.93 mMol) 4-benzyloxyphenylhydrazine hydrochloride in 80 mL ethanol were added 1.05 mL (12.93 mMol) pyridine. The resulting mixture was heated to 50° C. for about 20 minutes and then 1.87 mL (11.75 mMol) ethyl 4-oxocyclohexanecarboxylate were added. The resulting mixture was stirred at reflux for 18 hours. The reaction mixture was then concentrated under reduced pressure and the residue partitioned between water and ethyl acetate. The organic phase was separated, washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 35% ethyl acetate in hexane. Fractions containing product were combined and concentrated under reduced pressure to give 3.38 gm (83%) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05708187
Source datasetuspto-grants-1998_01
ORD IDord-3cb6a2c3073743f1a8ae250a66f49c87
Source noteuspto-grants-1998_01