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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642028Generated: October 31, 2026

Sodium triacetoxyborohydride → HCID 86633670, compound

https://huagongshe.com/reaction/1642028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(2-Methoxyethoxy)benzaldehydeHCID 6485560—
Reactant4-{Bis[4-(trifluoromethoxy)phenyl]methyl}piperidin-4-olHCID 16656274—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86633670HCID 8663367073.4%

Reaction Steps

A solution of 2.2 grams (0.0050 mole) of 4-{bis[4-(trifluoromethoxy)phenyl]methyl}piperidin-4-ol, 1.1 grams (0.0061 mole) of 4-(2-methoxyethoxy)benzaldehyde and 1.35 grams (0.0064 mole) of sodium triacetoxyborohydride in 25 mL of methylene chloride was stirred at ambient temperature for 18 hours. The reaction mixture was then diluted with 200 mL of water and stirred at ambient temperature for 5 hours. The phases were separated. The organic phase was washed three times; first, with 100 mL of an aqueous mixture of 10% sodium hydroxide, second, with 100 mL of an aqueous mixture of 10% lithium chloride, and, third, with 100 mL of brine. The resultant organic layer was dried over magnesium sulfate, filtered and concentrated under reduced pressure to a residue. The residue was purified with column chromatography on silica gel using methylene chloride:1%-5% methanol as an eluant. The appropriate fractions were combined and concentrated under reduced pressure, yielding 2.2 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119563B2
Source datasetuspto-grants-2012_02
ORD IDord-b71c28e5306043eb965408b4d722722f
Source noteuspto-grants-2012_02