Basic information Safety Supplier Related

1-N-BOC-3-IODOMETHYLPIPERIDINE

Basic information Safety Supplier Related

1-N-BOC-3-IODOMETHYLPIPERIDINE Basic information

Product Name:
1-N-BOC-3-IODOMETHYLPIPERIDINE
Synonyms:
  • CIVENTICHEM CV-5056
  • 1-BOC-3-IODOMETHYLPIPERIDINE
  • 1-N-BOC-3-IODOMETHYLPIPERIDINE
  • tert-butyl 3-(iodomethyl)piperidine-1-carboxylate
  • 3-(Iodomethyl)-1-piperidinecarboxylic acid tert-butyl ester
  • tert-Butyl 3-(iodomethyl)
  • N-BOC-3-(iodomethyl)piperidine
  • 1-Piperidinecarboxylic acid, 3-(iodomethyl)-, 1,1-dimethylethyl ester
CAS:
253177-03-6
MF:
C11H20INO2
MW:
325.19
Mol File:
253177-03-6.mol
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1-N-BOC-3-IODOMETHYLPIPERIDINE Chemical Properties

Boiling point:
336.6±15.0 °C(Predicted)
Density 
1.447
storage temp. 
2-8°C(protect from light)
pka
-1.92±0.40(Predicted)
Appearance
Colorless to light yellow Solid-liquid mixture
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1-N-BOC-3-IODOMETHYLPIPERIDINE Usage And Synthesis

Synthesis

116574-71-1

253177-03-6

General procedure for the synthesis of N-Boc-3-iodomethylpiperidine from tert-butyl 3-(hydroxymethyl)piperidine-1-carboxylate: Imidazole (1.58 g, 23.2 mmol), triphenylphosphine (6.09 g, 23.2 mmol), and iodine (4.72 g, 18.6 mmol) were sequentially added to a solution containing 1-(tert-butoxycarbonyl)piperidin-3-ylmethanol (2.00 g, 9.29 mmol) in a solution of benzene (50 mL). The reaction mixture was stirred at room temperature for 3 hours. Upon completion of the reaction, the mixture was filtered through diatomaceous earth and the filtrate was concentrated under reduced pressure. Water was added to the residue and subsequently extracted with ethyl acetate. The organic phases were combined, washed with saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent ratio: hexane/ethyl acetate = 20:1 → 5:1) to afford 2.91 g (96% yield) of the target compound N-Boc-3-iodomethylpiperidine as a light yellow oil. The product was confirmed by 1H NMR (400 MHz, CDCl3): δ 1.19-1.28 (1H, m), 1.40-1.52 (10H, m), 1.61-1.68 (2H, m), 1.91-1.95 (1H, m), 2.54-2.69 (1H, m), 2.79-2.84 (1H, m), 3.08 (2H , d, J=6.7 Hz), 3.84 (1H, td, J=13.4, 3.7 Hz), 3.97-4.13 (1H, m). Mass spectrometry analysis (FAB+) showed the molecular ion peak m/z: 326 ([M+H]+).

References

[1] Patent: EP1780210, 2007, A1. Location in patent: Page/Page column 54-55
[2] Bioorganic and Medicinal Chemistry Letters, 1997, vol. 7, # 12, p. 1525 - 1530
[3] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 21, p. 3235 - 3238
[4] Patent: US6335324, 2002, B1. Location in patent: Page column 211

1-N-BOC-3-IODOMETHYLPIPERIDINESupplier

Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
Amber MolTech LLC
Tel
086-010-62176588
Email
amber@jyamber.com
Shanghai Synthfine Chemical Co.,Ltd
Tel
15921303235
Email
sales@synthfine.com
Nanjing Norris-Pharm Technology Co., Ltd
Tel
18652989687
Email
sales@norris-pharm.com
Shanghai Jian Chao Chemical Technology Co., Ltd.
Tel
150-2103-5486 18017383231
Email
983544897@qq.com
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