| Identification | Back Directory | [Name]
4-PHENYLPIPERIDINE HYDROCHLORIDE | [CAS]
10272-49-8 | [Synonyms]
4-Phenylpiperdine HCL 4-phenylpiperidinium chloride 4-Phenylpiperdine hydrochloride 4-PHENYLPIPERIDINE HYDROCHLORIDE Piperidine, 4-phenyl-,hydrochloride (1:1) 1,2,3,6-Tetrahydro-4-phenylpiperidine hydrochloride | [EINECS(EC#)]
233-617-0 | [Molecular Formula]
C11H16ClN | [MDL Number]
MFCD01632527 | [MOL File]
10272-49-8.mol | [Molecular Weight]
197.7 |
| Chemical Properties | Back Directory | [Melting point ]
164-165℃ | [storage temp. ]
Inert atmosphere,Room Temperature | [Appearance]
White to off-white Solid | [InChI]
InChI=1S/C11H15N.ClH/c1-2-4-10(5-3-1)11-6-8-12-9-7-11;/h1-5,11-12H,6-9H2;1H | [InChIKey]
UPZJLQCUYUTZIE-UHFFFAOYSA-N | [SMILES]
C1(C=CC=CC=1)C1CCNCC1.Cl |
| Hazard Information | Back Directory | [Chemical Properties]
mp 154-158°C | [Synthesis]
The general procedure for the synthesis of 4-phenylpiperidine hydrochloride from 4-phenyl-1,2,3,6-tetrahydropyridine hydrochloride was as follows: 10% palladium carbon (100 mg) was added to a stirred solution of 4-phenyl-1,2,3,6-tetrahydropyridine hydrochloride (300 mg, 1.53 mmol) in methanol (10 mL) under argon protection. Subsequently, the reaction mixture was flushed with hydrogen three times and the reaction was stirred under hydrogen atmosphere (balloon) for 4 hours. The reaction progress was monitored by LCMS. After completion of the reaction, the reaction mixture was filtered through a short diatomaceous earth pad and washed with methanol (5 mL). The filtrate was concentrated under reduced pressure and the residue was washed with anhydrous ether (2 x 5 mL) to give the final 4-phenylpiperidine hydrochloride (300 mg, 99%) as an off-white hygroscopic solid. m/z 162.3 [M+H]+ by LCMS. | [References]
[1] Patent: US2003/171370, 2003, A1 [2] Patent: WO2018/125961, 2018, A1. Location in patent: Page/Page column 42; 43 [3] Patent: US2004/92524, 2004, A1. Location in patent: Page/Page column 38 [4] Patent: US6355642, 2002, B1. Location in patent: Page column 14 [5] Patent: EP1020434, 2000, A1 |
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