Diethyl Ether → 2-Methyl-1-(piperidin-4-yl)propan-2-ol

To a solution of 0.69 g (2.7 mmol) of 1-t-butoxycarbonyl-4-(methoxycarbonylethyl)piperidine (Example 22, Step 2) in 26 mL of ether at 0° C. was added dropwise 2.8 mL (8.4 mmol) of CH3MgBr (3 M in ether) and the reaction mixture was warmed slowly to rt. After stirring at rt for 6 h, the reaction was quenched by addition of 20 mL of sat'd NH4Cl solution and the mixture was stirred overnight. The mixture was extracted with ethyl acetate. The combined organic fractions were washed with sat'd NaCl solution, dried over MgSO4, filtered and the filtrate was concentrated. The residue was purified by chromatography (silica, hexanes-:ethyl acetate, 3:1) to give 0.5 g of the title compound.

1. customthe reaction was quenched by addition of 20 mL of sat'd NH4Cl solution
2. stirringthe mixture was stirred overnight
3. extractionThe mixture was extracted with ethyl acetate
4. washThe combined organic fractions were washed with sat'd NaCl solution
5. dry with materialdried over MgSO4
6. filtrationfiltered
7. concentrationthe filtrate was concentrated
8. customThe residue was purified by chromatography (silica, hexanes-:ethyl acetate, 3:1)

ORD record

ord-18e9b361be87475c8b28a056ef5c2ec7

Source dataset

uspto-grants-2002_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06455548B2