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ChemicalBook CAS DataBase List cis-2,6-Dimethyl-4-oxo-piperidine-1-carboxylic acid tert-butyl ester
1005397-64-7

cis-2,6-Dimethyl-4-oxo-piperidine-1-carboxylic acid tert-butyl ester synthesis

2synthesis methods
24424-99-5 Synthesis
Di-tert-butyl dicarbonate

24424-99-5
833 suppliers
$13.50/25G

13200-35-6 Synthesis
(2S,6R)-2,6-dimethylpiperidin-4-one

13200-35-6
34 suppliers
$180.00/50mg

cis-2,6-Dimethyl-4-oxo-piperidine-1-carboxylic acid tert-butyl ester

1005397-64-7
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Yield:1005397-64-7 73%

Reaction Conditions:

with N-ethyl-N,N-diisopropylamine in dichloromethane at 20; for 12 h;

Steps:

5.C Step C: tert-butyl-cis-2,6-dimethyl-4-oxopiperidine- 1 -carboxylate.
Di-tert-butyl dicarbonate (3.14 g, 14.4 mmol) and N,N-diisopropylethylamine (3.124 mmol) were added to a solution of cis- 1 -(4-methoxybenzyl)-2,6-dimethylpiperidin- 4-one (1.54 g, 12 mmol) in dichloromethane (30 mL) and the mixture was stirred at room temperature for 12 hr. Solvent was removed under reduced pressure and the residue was purified by silica gel chromatography with hexane/ethyl acetate (8/2, v/v) to afford thecompound (2.0 g, 73 % yield) as a white solid. ‘H NIvIR (400 MHz, CDC13) 4.41- 4.39 (m, 2H), 2.85 (dd, J= 17.8, 6.5 Hz, 2H), 2.37 (dd, J= 17.8, 1.9 Hz, 2H), 1.50 (s, 9H), 1.25 (d, J= 6.8 Hz, 6H).

References:

THE REGENTS OF THE UNIVERSITY OF MICHIGAN;WANG, Shaomeng;CHEN, Jianyong WO2018/44767, 2018, A2 Location in patent:Paragraph 0174; 0175

FullText

198211-15-3 Synthesis
RZABKAGQMPNUFJ-TXEJJXNPSA-N

198211-15-3
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cis-2,6-Dimethyl-4-oxo-piperidine-1-carboxylic acid tert-butyl ester

1005397-64-7
37 suppliers
inquiry

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