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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176408Generated: October 29, 2026

Sodium ethoxide → HCID 58336756, compound

https://huagongshe.com/reaction/2176408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 58336735HCID 58336735—
ReactantHCID 85361696HCID 85361696—
SolventEthanolHCID 702—
ProductHCID 58336756HCID 58336756—

Reaction Steps

Under argon, 0.73 g (2.7 mmol) of 6-(1-pyridin-3-yl-1H-pyrazol-4-yl)pyridine-2-carboxamidine and 0.8 g (2.9 mmol) of (3-dimethylaminoallylidene)dimethylammonium hexafluorophosphate in 30 ml of ethanol were heated under reflux with 3 ml of sodium ethoxide as a solution in ethanol (21%, corresponds to 8.1 mmol) for 6 h. The mixture was concentrated, Na citrate buffer, dil. aqueous sodium hydroxide solution to pH=9, aq. NaCl and ethyl acetate/THF were added, the aqueous phase was extracted three more times with dichloromethane/2-propanol and the combined organic phases were dried with MgSO4 and concentrated by evaporation. The residue was recrystallized from ethanol, during this operation, the mixture was briefly boiled with activated carbon and filtered whilst still hot, the filtrate was concentrated slightly and the precipitate formed was washed with MTBE and dried on a rotary evaporator. The residue was purified further by filtration through silica gel using acetone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09066518B2
Source datasetuspto-grants-2015_06
ORD IDord-f8d561fdd6df45a4a78ed3ac31fe94b3
Source noteuspto-grants-2015_06