3-Phenylpiperidine

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3-Phenylpiperidine manufacturers

  • 3-Phenylpiperidine
  • 3-Phenylpiperidine pictures
  • $1.00
  • 2020-02-17
  • CAS:3973-62-4
  • Min. Order: 1KG
  • Purity: 98% HPLC
  • Supply Ability: 10 tons
3-Phenylpiperidine Basic information
Product Name:3-Phenylpiperidine
Synonyms:TIMTEC-BB SBB010187;CHEMBRDG-BB 4003675;3-phenylpiperidine(SALTDATA: FREE);(Piperidin-3-yl)benzene;ChemDiv2_003191;EINECS 223-602-7;Piperidine, 3-phenyl-;SBB010187
CAS:3973-62-4
MF:C11H15N
MW:161.24
EINECS:223-602-7
Product Categories:Piperidine
Mol File:3973-62-4.mol
3-Phenylpiperidine Structure
3-Phenylpiperidine Chemical Properties
Melting point 142-143℃
Boiling point 121°C/9mm
density 0.967
refractive index 1.5256
Fp 116℃
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka10.01±0.10(Predicted)
form clear liquid
color Colorless to Almost colorless
InChIInChI=1S/C11H15N/c1-2-5-10(6-3-1)11-7-4-8-12-9-11/h1-3,5-6,11-12H,4,7-9H2
InChIKeyNZYBILDYPCVNMU-UHFFFAOYSA-N
SMILESN1CCCC(C2=CC=CC=C2)C1
CAS DataBase Reference3973-62-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-36
Safety Statements 26-36/37/39
WGK Germany WGK 3
HazardClass IRRITANT
HS Code 2933399990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
MSDS Information
3-Phenylpiperidine Usage And Synthesis
Chemical PropertiesWhite crystalline powder
Synthesis
1-benzyl-3-phenylpiperidine

3979-67-7

3-PHENYLPIPERIDINE

3973-62-4

N-benzyl-3-phenylpiperidine (3-1, 65 g, 258.96 mmol) was added palladium carbon (12 g, 18%), anhydrous ethanol (300 mL) and glacial acetic acid (11 mL) in a reaction flask. The reaction was heated to 60 °C for 12 h under 1 atm hydrogen atmosphere. The reaction progress was monitored by TLC and stopped after confirming the complete reaction of the ingredients. The reaction mixture was filtered to remove palladium carbon and the filtrate was concentrated to dryness by rotary evaporation. The residue was dissolved in water (250 mL) and extracted with ethyl acetate (250 mL x 3), the organic layers were combined and dried over anhydrous sodium sulfate. After filtration, the solvent was removed by rotary evaporation to afford 35.2 g of 3-phenylpiperidine (1) in 89.3% yield, and the product was used directly in the subsequent reaction.

References[1] Patent: CN108203404, 2018, A. Location in patent: Paragraph 0223-0226
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