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

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

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
EINECS:
Product Categories:API intermediates
Mol File:163271-08-7.mol
tert-Butyl (4-methylpiperidin-4-yl)carbamate Structure
tert-Butyl (4-methylpiperidin-4-yl)carbamate Chemical Properties
Boiling point 308 °C
density 1.01
Fp 140 °C
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka12.75±0.20(Predicted)
form powder
color Gray
InChIInChI=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)
InChIKeyMVUNGZMGWJXPIM-UHFFFAOYSA-N
SMILESC(OC(C)(C)C)(=O)NC1(C)CCNCC1
Safety Information
HS Code 2933399990
MSDS Information
tert-Butyl (4-methylpiperidin-4-yl)carbamate Usage And Synthesis
Usestert-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
tert-butyl 1-benzoyl-4-methylpiperidin-4-ylcarbamate

1262787-56-3

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

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
tert-Butyl (4-methylpiperidin-4-yl)carbamate Preparation Products And Raw materials
Raw materialstert-butyl 1-benzoyl-4-methylpiperidin-4-ylcarbamate-->Water-->Sodium hydroxide-->Ethanol
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