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153108-65-7

(S)-1-Boc-2-acetyl-piperidine synthesis

2synthesis methods
-

Yield:153108-65-7 96%

Reaction Conditions:

in tetrahydrofuran at -10; for 3.5 h;Inert atmosphere;

Steps:

1.2 Synthesis of (S)-1-(tert-butoxycarbonyl)-2-acetylpiperidine 3:

Under the protection of nitrogen,dissolve 10.6 g (38.9 mmol) of compound 2 in 200 mL of tetrahydrofuran,Cool to -10°C,slowly add 32.5mL (97.3mmol) 3M methylmagnesium bromide dropwise,after 3.5 hours of reaction,add 30mL saturated aqueous ammonium chloride solution,the reaction solution was extracted with ether (60mL×3),Dry with anhydrous sodium sulfate,filter,remove the solvent under reduced pressure,Column chromatography separation,V (petroleum ether): V (ethyl acetate) = 3:1,Get 8.5g colorless oily liquid,The yield was 96%.

References:

CN111689957,2020,A Location in patent:Paragraph 0038; 0043-0046