Hydrochloric Acid → 1-Benzyl-4-(trifluoromethyl)piperidin-4-ol

温度

0 °C

A mixture of 1-benzyl-4-piperidone (2.2 g, 11.67 mmole) and (trifluoromethyl)-trimethyl silane (2.37 g, 16.7 mmole) in dry THF (10 ml) at 0° C. was treated with tetrabutylammonium fluoride (0.02 g) in THF. The mixture was stirred at 0° C. for 15 min and allowed to stir at 25-30° C. for 2 hr. THF (10 ml) and 3N HCl were added and stirred for 2 hr. The reaction mixture was extracted with ethyl acetate (3×25 ml), washed with water (2×10 ml) and brine (20 ml), dried (Na2SO4). Residue obtained after evaporation of solvent was purified by column chromatography over silica gel. Elute from a mixture of 5% methanol in chloroform gave 1-benzyl-4-hydroxy-4-trifluoromethylpiperidine as an oil. Yield 2.2 g, (73%), C13H24NOF3, m/z 260 (M+1), PMR (CDCl3): 1.7 (2H, d, CH2, j=10 Hz), 1.85 (1H, bs, OH, D2O exchangeable), 1.9 (2H, t, CH2, j=10 Hz), 2.3 (2H, t, CH2, j=10 Hz), 2.8 (2H, d, CH2, j=10 Hz), 3.55 (2H, s, CH2Ar), 7.2-7.4 (5H, m, ArH).

1. stirringto stir at 25-30° C. for 2 hr
2. stirringstirred for 2 hr
3. extractionThe reaction mixture was extracted with ethyl acetate (3×25 ml)
4. washwashed with water (2×10 ml) and brine (20 ml)
5. dry with materialdried (Na2SO4)
6. customResidue obtained
7. customafter evaporation of solvent
8. customwas purified by column chromatography over silica gel
9. washElute from a mixture of 5% methanol in chloroform

ORDレコード

ord-f5bd7c40815e4dca950b9d8360512a2c

出典データセット

uspto-grants-2003_08

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06608078B2