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1314396-07-0

5-Hydroxy-2-Methyl-Piperidine-1-Carboxylic Acid Benzyl Ester synthesis

4synthesis methods
-

Yield:1314396-07-0 42%

Reaction Conditions:

with triethylamine in dichloromethane; for 16 h;

Steps:

121.2 Step 2: preparation of benzyl 5-hydroxy-2-methylpiperidine-i-carboxylate.

Step 2: preparation of benzyl 5-hydroxy-2-methylpiperidine-i-carboxylate. To a solution of 6-methylpiperidin-3-ol (9.0 g, 78.1 mmol) in dichloromethane (100 mL) wasadded drop wise triethylamine (101 mL, 703 mmol), followed by benzyl chloroformate (14 mL, 93.8 mmol). The reaction was allowed to stir over 16h, after which it was concentrated in vacuo, and the resulting residue purified by silica gel column chromatography to afford the title compound as colorless oil (8.ig 42%).

References:

WO2014/68527,2014,A1 Location in patent:Page/Page column 150

1314395-91-9 Synthesis
benzyl 2-methyl-5-oxopiperidine-1-carboxylate

1314395-91-9
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$45.00/10mg