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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919712Generated: November 2, 2026

Lithium Carbonate → HCID 22620205, compound

https://huagongshe.com/reaction/1919712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium CarbonateHCID 11125—
ReactantHCID 22620178HCID 22620178—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 22620205HCID 22620205—

Reaction Steps

To a stirred solution of 1-(tert-Butoxycarbonyl)-4-chloro-6-methyl-2-cyclopentyl-1,2-dihydropyridine (2.54 g, 8.53 mmol) in 175 mL of MeOH at 0° C. was added of lithium carbonate (0.63 g, 8.53 mmol) followed by 5% Pd/C. The mixture was placed under a positive pressure of hydrogen gas from a balloon, and the reaction progress was monitored by removing aliquots with a syringe, concentrating the aliquot in vacuo, and examining its 1H NMR spectrum. Upon completion, the mixture was filtered through Celite and evaporated. The residue was dissolved in ether (100 mL) and water (50 mL) was added, and the aqueous phase was extracted twice with ether. The combined organic extracts were washed with 1M NaOH and brine. The organic phase was dried with potassium carbonate, filtered through Celite, and concentrated in vacuo to give the crude product. Purification by column chromatography (silica gel, 5% EtOAc in hexanes) afforded 1.14 g (52%) as a clear oil that was homogeneous by TLC analysis. 1H NMR (300 MHz) δ 4.87 (br s, 1H), 4.45-4.40 (m, 1H), 2.22, (m, 1H), 2.02 (s, 3H), 1.99-1.91 (m, 2H), 1.82-1.20 (m, 21H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168657B2
Source datasetuspto-grants-2012_05
ORD IDord-77f518bdf9384b1e88341e318451640c
Source noteuspto-grants-2012_05