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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074313Generated: October 29, 2026

Pyridine → HCID 70372059, compound

https://huagongshe.com/reaction/1074313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 13590075HCID 13590075—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
CatalystLindlars catalystHCID 131709914—
SolventEthyl AcetateHCID 8857—
ProductHCID 70372059HCID 7037205999.3%

Reaction Steps

cis-hydrogenation using Lindlar catalyst and pyridine: Stir a mixture of 533 mg, 2.51 mmoles of the title compound of Example 1 (recrystallized from dichloromethane-hexane), 211 mg, 2.67 mmoles of pyridine and 127 mg of Lindlar catalyst (palladium on calcium carbonate, poisoned with lead (obtained from Aldrich) in 25 mL of ethyl acetate under hydrogen at atomospheric pressure at 26° C. for 1 hr until the theoretical amount of hydrogen (62 mL) is consumed. Remove the catalyst by filtration and wash it with ethyl acetate. Wash the ethyl acetate solution successively with ice-cold 4% HCl solution, saturated NaHCO3 solution and water, and dry over anhydrous MgSO4. Evaporate solvent under vacuum to give the title compound as an oil (534 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04973750
Source datasetuspto-grants-1990_11
ORD IDord-0bff7090d48d4070adf006504660b498
Source noteuspto-grants-1990_11