HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642028Generated: October 31, 2026
Sodium triacetoxyborohydride → HCID 86633670, compound
https://huagongshe.com/reaction/1642028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 4-(2-Methoxyethoxy)benzaldehyde | HCID 6485560 | — |
| Reactant | 4-{Bis[4-(trifluoromethoxy)phenyl]methyl}piperidin-4-ol | HCID 16656274 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86633670 | HCID 86633670 | 73.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119563B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-b71c28e5306043eb965408b4d722722f |
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| Source note | uspto-grants-2012_02 |
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