HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100670Generated: October 31, 2026
Boron tribromide → 4-Piperidin-1-yl-3-trifluoromethyl-phenol
https://huagongshe.com/reaction/2100670
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(4-Methoxy-2-trifluoromethyl-phenyl)-piperidine | HCID 68812212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Piperidin-1-yl-3-trifluoromethyl-phenol | HCID 68813128 | — |
Reaction Steps
To a solution of crude 1-(4-Methoxy-2-trifluoromethyl-phenyl)-piperidine in dry DCM (3 mL) cooled to −78° C. is added BBr3 (1M in DCM, 3 eq., 1.2 mL). Following this addition, the cooling bath is removed and the reaction is stirred at 25° C. for 12 hours. Upon completion, the reaction is cooled in an ice bath, and water is added dropwise. The quenched reaction is basified to pH=8 by the slow addition of 10% NaHCO3 (aq). The reaction mixture is diluted with DCM and washed with H2O followed by saturated aqueous NaCl. The organic solution is dried over Na2SO4. After concentration, the residue is purified by silica gel chromatography (3:1 hexanes/EtOAc) to give 4-Piperidin-1-yl-3-trifluoromethyl-phenol. [MS: (ES+) 246.1 (M+1)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572811B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-dc7768751a3f45d1aac363a7059fdbf2 |
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| Source note | uspto-grants-2009_08 |
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