Basic information Safety Supplier Related

1-BOC-4-(4-BROMO-BENZOYL)-PIPERIDINE

Basic information Safety Supplier Related

1-BOC-4-(4-BROMO-BENZOYL)-PIPERIDINE Basic information

Product Name:
1-BOC-4-(4-BROMO-BENZOYL)-PIPERIDINE
Synonyms:
  • 1-BOC-4-(4-BROMO-BENZOYL)-PIPERIDINE
  • tert-butyl 4-(4-broMobenzoyl)piperidine-1-carboxylate
  • tert-butyl 4-[(4-broMophenyl)carbonyl]piperidine-1-carboxylate
  • 1-Piperidinecarboxylic acid, 4-(4-bromobenzoyl)-, 1,1-dimethylethyl ester
  • 4-(4-bromobenzoyl)piperidine-1-carboxylic acid tert-butyl ester
CAS:
439811-37-7
MF:
C17H22BrNO3
MW:
368.27
EINECS:
200-589-5
Mol File:
439811-37-7.mol
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1-BOC-4-(4-BROMO-BENZOYL)-PIPERIDINE Chemical Properties

Boiling point:
452.3±40.0 °C(Predicted)
Density 
1.325±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
-2.47±0.40(Predicted)
Appearance
Off-white to light yellow Solid
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1-BOC-4-(4-BROMO-BENZOYL)-PIPERIDINE Usage And Synthesis

Synthesis

746550-66-3

24424-99-5

439811-37-7

Step 1. Synthesis of tert-butyl 4-(4-bromobenzoyl)-piperidine-1-carboxylate. To a 250 mL round bottom flask was added 4-(4-bromobenzoyl)piperidine (5 g, 20 mmol), tetrahydrofuran (30 mL), water (30 mL), sodium carbonate (10 g, 90 mmol) and di-tert-butyl dicarbonate (4.35 g, 20.0 mmol). The reaction mixture was stirred at room temperature for 2 h and then partitioned with ethyl acetate and water. The aqueous layer was extracted twice with ethyl acetate, the organic phases were combined, washed with brine, dried, filtered and concentrated to give 7.1 g (100% yield) of tert-butyl 4-(4-bromobenzoyl)-piperidine-1-carboxylate.

References

[1] Patent: WO2016/205590, 2016, A1. Location in patent: Paragraph 00596
[2] Patent: WO2013/147711, 2013, A1. Location in patent: Page/Page column 231
[3] Patent: US2014/371199, 2014, A1. Location in patent: Paragraph 0801
[4] Patent: US2005/54628, 2005, A1. Location in patent: Page/Page column 23-24
[5] Patent: US2005/49269, 2005, A1. Location in patent: Page/Page column 12; 21

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