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1-(1-Benzylpiperidin-4-yl)pyrrolidin-2-one synthesis

5synthesis methods
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Yield:340962-88-1 94.6%

Reaction Conditions:

Stage #1: 1-phenylmethyl-4-piperidone;ethyl γ-aminobutyrate hydrochloridewith sodium tris(acetoxy)borohydride for 1.5 h;
Stage #2: with triethylamine at 20 - 60; for 21 h;Solvent;Temperature;Time;

References:

Mapes, Christopher M.;Mani, Neelakandha S. [Organic Process Research and Development,2007,vol. 11,# 3,p. 482 - 486] Location in patent:supporting information

50541-93-0 Synthesis
4-Amino-1-benzylpiperidine

50541-93-0
366 suppliers
$6.00/5g

2969-81-5 Synthesis
Ethyl 4-bromobutyrate

2969-81-5
446 suppliers
$5.00/1g

1-(1-Benzylpiperidin-4-yl)pyrrolidin-2-one

340962-88-1
8 suppliers
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