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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856026Generated: October 30, 2026

Hydrochloric Acid → 1-[4-(Trifluoromethoxy)phenyl]piperidin-4-ol

https://huagongshe.com/reaction/856026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant1-[4-(Trifluoromethoxy)phenyl]piperidin-4-oneHCID 23081588—
SolventMethanolHCID 887—
Product1-[4-(Trifluoromethoxy)phenyl]piperidin-4-olHCID 2308157097%

Reaction Steps

Sodium borohydride (324 mg, 8.56 mmol) was added to a solution of 1-(4-trifluoromethoxyphenyl) piperidin-4-one (1.11 g, 4.28 mmol) prepared in Reference Example 22 in methanol (30 ml) while cooling in an ice-bath, and the mixture was stirred for 30 minutes. To which 10% hydrochloric acid was added, and the resulting mixture was concentrated under reduced pressure. To the residue saturated sodium bicarbonate aqueous solution was added, and the mixture was extracted with methylene chloride. The extract was washed with water and brine, and dried over magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=3/1) to afford 1-(4-trifluoromethoxyphenyl)piperidin-4-ol (1.08 g, yield 97%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-4070bf017c504f78b2ab31c14a247b12
Source noteuspto-grants-2007_08