ChemicalBook CAS DataBase List N-Boc-3-carboethoxy-4-piperidone

N-Boc-3-carboethoxy-4-piperidone synthesis

10synthesis methods

Product Name:N-Boc-3-carboethoxy-4-piperidone
CAS Number:98977-34-5
Molecular formula:C13H21NO5
Molecular Weight:271.31

24424-99-5 Synthesis

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

Ethyl 1-benzyl-4-oxo-3-piperidinecarboxylate hydrochloride

1454-53-1
247 suppliers
$5.00/5g

98977-34-5
199 suppliers
$5.00/250mg

Yield:98977-34-5 100%

Reaction Conditions:

Stage #1: ethyl 1-benzyl-4-oxopiperidine-3-carboxylate hydrochloridewith hydrogen;palladium 10% on activated carbon in ethanol at 20; under 760.051 Torr; for 15 h;
Stage #2: di-tert-butyl dicarbonatewith triethylamine in ethanol at 20; for 16 h;

Steps:

1; 1.1

A solution of l-benzyl-3-carboethoxy-4-piperidone hydrochloride (IA) (10.0 g, 33.6 mmol) in ethanol (800 mL) and Pd/C (1.0 g, 10% w/w) was hydrogenated at 1 arm. for about 15 hours at room temperature. After the reaction was complete, triethylamine (19 mL, 134.3 mmol) and (Boc)₂O (8.0 g, 36.9 mmol) were added to the mixture. The resulting solution was stirred at room temperature for 16 hours and the catalyst was removed by filtering through Celite. The filtrate was concentrated in vacuo, the resulting residue was dissolved in dichloromethane and extracted by washing with water. The organic phase was separated and dried over Na₂SO₄ and concentrated in vacuo to provide compound IB (9. Ig, 100%).

References:

WO2008/130584,2008,A1 Location in patent:Page/Page column 131; 135

24424-99-5 Synthesis

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

4644-61-5 Synthesis