HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232930Generated: October 25, 2026
1-Benzyl-4-piperidone → 1-Benzyl-4-[4-chloro-3-(trifluoromethyl)phenyl]-4-piperidinol
https://huagongshe.com/reaction/2232930
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | 4-Bromo-2-chloro-alpha,alpha,alpha-trifluorotoluene | HCID 67959 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Benzyl-4-[4-chloro-3-(trifluoromethyl)phenyl]-4-piperidinol | HCID 22345180 | 64% |
Reaction Steps
A solution of 5-Bromo-2-chlorobenzotrifluoride (5 g, 19.2 mmol) in dry diethyl ether (40 ml) was added dropwise at room temperature to a mixture of Mg (470 mg) in dry diethyl ether (20 ml) under a stream of Argon (g). The reaction gave rise to a solution of Grignard's reagent. A solution of 1-benzyl-4-piperidone (1.3 g, 6.88 mmol) in dry diethyl ether (30 ml) was added dropwise via syringe at room temperature. The combined mixture was stirred for 1 hour, and finally quenched with saturated ammonium chloride solution (40 ml). The mixture was extracted several times with EtOAc and the combined organic phases were dried (MgSO4), filtered and evaporated to dryness. The oily residue was chromathographed on a silica column using EtOAc:toluene (1:1 (v/v)) as eluent affording the title compound (1.6 g, 64%). MS m/z (relative intensity, 70 eV) 369 (M+, 23), 278 (15), 91 (bp), 65 (16), 56 (21).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | USRE041315E1 |
|---|
| Source dataset | uspto-grants-2010_05 |
|---|
| ORD ID | ord-25e77246674f4f29b03a7d9940ce5b9e |
|---|
| Source note | uspto-grants-2010_05 |
|---|