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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159337Generated: October 31, 2026

Citric Acid → HCID 67505370, compound

https://huagongshe.com/reaction/1159337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantPotassium CarbonateHCID 11430—
ReactantChlorosuccinimideHCID 31398—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67505621HCID 67505621—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventDichloromethaneHCID 6344—
ProductHCID 67505370HCID 67505370—

Reaction Steps

5-(4-Chloro-phenyl)-N-((1R,2R)-2-hydroxy-cyclohexyl)-6-(5-hydroxy-pentyloxy)-nicotinamide (0.23 g, 0.5 mmol) was dissolved in dichloromethane (15 mL). To the solution was added 2,2,6,6-tetramethyl-1-piperidinyloxy (1 mg), tetrabutylammoniumchlorid (1.5 mg), 5 mL of an aqueous solution of sodium bicarbonate (0.5 M) and potassium carbonate (0.05 M) and N-chlorosuccinimid (0.146 g, 1.1 mmol). The mixture was stirred for 72 h at room temperature and afterwards poured into citric acid (10%, 20 mL) and extracted with dichloromethane. Organic phases were pooled, dried with Na2SO4 and the solvent was evaporated. The residue (aldehyde contaminated with some starting alcohol) was redissolved in tert-butanol (5 mL). To the solution was added 2-methyl-butene solution (2 M in THF, 5 mL), sodium chlorite (210 mg), and sodium dihydrogenphosphate (0.345 g). The mixture was stirred for 72 h at room temperature and afterwards poured into citric acid (10%, 50 mL) and extracted with ethyl acetate. Organic phases were pooled, dried with MgSO4 and the solvent was evaporated. The residue was purified by column chromatography on silica (dichloromethane/methanol gradient) to yield 0.062 g of the title compound as a white foam, MS (ISP) 445.2 (M−H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812028B2
Source datasetuspto-grants-2010_10
ORD IDord-bc57a42019334203a5b522df4022f9a8
Source noteuspto-grants-2010_10