반응 #2306092

반응 방정식

4-[5-fluoro-2-(3,3,5,5-tetramethylcyclohex-1-enyl)phenyl]piperidine-1-carboxylic acid t-butyl ester

trifluoroacetic acid

→

crude product

수율 118.2%

4-[5-Fluoro-2-(3.3, 5,5-tetramethylcyclohex-1-enyl)phenyl]piperidine

수율 118.2%

용매

dichloromethane

반응 조건

후처리

1. 1
   농축The reaction mixture was concentrated under reduced pressure
2. 2
   workup.ADDITIONsaturated aqueous solution of sodium hydrogencarbonate was added to the obtained residue and extraction
3. 3
   건조The organic layer was dried over anhydrous magnesium sulfate
4. 4
   농축the filtrate was concentrated under reduced pressure

실험 절차

To a solution of 4-[5-fluoro-2-(3,3,5,5-tetramethylcyclohex-1-enyl)phenyl]piperidine-1-carboxylic acid t-butyl ester (245 mg, 0.59 mmol) produced in Example (106f) in dichloromethane (3 mL) was added trifluoroacetic acid (3 mL), followed by stirring for 30 minutes at room temperature. The reaction mixture was concentrated under reduced pressure, and then saturated aqueous solution of sodium hydrogencarbonate was added to the obtained residue and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the filtrate was concentrated under reduced pressure to give 220 mg of a crude product of the title compound as a light yellow solid.

출처