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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502982Generated: November 4, 2026

Sodium Bicarbonate → HCID 68468390, compound

https://huagongshe.com/reaction/502982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 68470240HCID 68470240—
ReactantHCID 178494172HCID 178494172—
SolventTolueneHCID 1140—
SolventChloroformHCID 6212—
ProductHCID 68468390HCID 6846839013.9%

Reaction Conditions

Temperature105 °C

Reaction Steps

(1E)-8-Methoxy-2,3,4,5,6,7-hexahydroazocine (614 mg) and p-toluenesulfonic acid monohydrate (207 mg) were added to a toluene (20 ml) solution of 1-cyclohexylcyclopentanecarbohydrazide (762 mg), followed by stirring at 105° C. for 3 days. The reaction solution and chloroform were added to a saturated aqueous sodium hydrogen carbonate solution and then the organic layer was separated. Furthermore, the organic layer washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered and then the solvent was removed by evaporation under reduced pressure. The resulting crude product was purified by flash column chromatography (chloroform:methanol=97:3) to obtain 152 mg of 3-(1-cyclohexylcyclopentyl)-5,6,7,8,9,10-hexahydro[1,2,4]triazolo[4,3-a]azocine (pale brown solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776897B2
Source datasetuspto-grants-2010_08
ORD IDord-4eeb8f77278b4b0d87539d4181e2f9cd
Source noteuspto-grants-2010_08