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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-[4-(Trifluoromethoxy)phenyl]piperidin-4-one | HCID 23081588 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[4-(Trifluoromethoxy)phenyl]piperidin-4-ol | HCID 23081570 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262212B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-4070bf017c504f78b2ab31c14a247b12 |
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| Source note | uspto-grants-2007_08 |
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