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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827286Generated: October 30, 2026

Acetic Acid → Sodium Bicarbonate

https://huagongshe.com/reaction/1827286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-oneHCID 70556—
Reactant2-BromonicotinaldehydeHCID 4714951—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductSodium BicarbonateHCID 516892—
ProductHCID 22136241HCID 22136241—

Reaction Steps

To a stirring solution of 2-bromo-pyridine-3-carbaldehyde (0.68 g, 3.6 mmol) were added 1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one (0.846 g, 3.6 mmol), and acetic acid (1.1 g, 18 mmol) in THF (40.0 ml) and sodium triacetoxyborohydride (1.55 g, 7.3 mmol) and the resulting reaction mixture stirred at room temperature overnight. Water (50 ml) was added and the reaction mixture solution was extracted with ethyl acetate three times. The combined organic layers were dried over MgSO4. The solvent was removed and the resulting residue was purified over silica gel column eluted with methylene chloride (97%), methanol (2%), acetic acid (1%) and then with saturated sodium bicarbonate solution to yield 8-(2-bromo-pyridin-3-ylmethyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053101B2
Source datasetuspto-grants-2006_05
ORD IDord-a24144b80e424a62913afa19b3c73302
Source noteuspto-grants-2006_05