Basic information Safety Supplier Related

tert-Butyl (4-methylpiperidin-4-yl)carbamate

Basic information Safety Supplier Related

tert-Butyl (4-methylpiperidin-4-yl)carbamate Basic information

Product Name:
tert-Butyl (4-methylpiperidin-4-yl)carbamate
Synonyms:
  • 4-Methylpiperidin-4-yl)carbami
  • (4-Methylpiperidin-4-yl)carbamic acid tert-butyl ester
  • tert-Butyl (4-methyl-4-piperidinyl)carbamate
  • (4-Methylpiperidin-4-yl)carbamic acid 1,1-dimethylethyl ester
  • tert-Butyl (4-methylpiperidin-4-yl)carbamate
  • 4-(Boc-amino)-4-methylpip...
  • 4-(Boc-aMino)-4-Methylpiperidine
  • tert-Butyl N-(4-Methyl-4-piperidyl)carbaMate
CAS:
163271-08-7
MF:
C11H22N2O2
MW:
214.3
Product Categories:
  • API intermediates
Mol File:
163271-08-7.mol
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tert-Butyl (4-methylpiperidin-4-yl)carbamate Chemical Properties

Boiling point:
308 °C
Density 
1.01
Flash point:
140 °C
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
12.75±0.20(Predicted)
form 
powder
color 
Gray
InChI
InChI=1S/C11H22N2O2/c1-10(2,3)15-9(14)13-11(4)5-7-12-8-6-11/h12H,5-8H2,1-4H3,(H,13,14)
InChIKey
MVUNGZMGWJXPIM-UHFFFAOYSA-N
SMILES
C(OC(C)(C)C)(=O)NC1(C)CCNCC1
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Safety Information

HS Code 
2933399990
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tert-Butyl (4-methylpiperidin-4-yl)carbamate Usage And Synthesis

Uses

tert-Butyl (4-methylpiperidin-4-yl)carbamate is versatile intermediates in organic synthesis, particularly in the pharmaceutical industry. They are used in the synthesis of various compounds, including natural products and potential therapeutic agents. 

Synthesis

1262787-56-3

163271-08-7

General procedure for the synthesis of tert-butyl (4-methylpiperidin-4-yl)carbamate from (1-benzoyl-4-methylpiperidin-4-yl)carbamate: 1. tert-Butyl (1-benzoyl-4-methylpiperidin-4-yl)carbamate (318 mg, 1.0 mmol) was dissolved in ethanol (3 mL). 2. 6 N aqueous sodium hydroxide (1.0 mL, 6.0 mmol) was added to the above solution. 3. The reaction mixture was heated at reflux for 8 hours. 4. 4. Upon completion of the reaction, the mixture was concentrated under reduced pressure. 5. Ethyl acetate (30 mL) was added to the concentrated mixture. 6. The organic layer was separated and washed twice with distilled water. 7. Dry the organic layer with anhydrous magnesium sulfate. 8. Concentrate the dried organic layer under reduced pressure and dry under reduced pressure to afford the target product tert-butyl (4-methylpiperidin-4-yl)carbamate (145 mg, 0.67 mmol, 67% yield). Characterization data: Mass spectrum (EI, m/z): 214 [M]+. 1H-NMR (CDCl3) δ: 4.37 (1H, br s), 2.84-2.80 (4H, m), 1.91 (2H, dt, J = 13.3, 3.9 Hz), 1.51 (2H, td, J = 12.9, 6.2 Hz), 1.44 (9H, s), 1.34 (3H, s).

References

[1] Patent: US2012/149902, 2012, A1. Location in patent: Page/Page column 24

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