Chlorotrimethylsilane → Benzeneethanamine, 3-fluoro-4-(trifluoromethyl)-

Chlorotrimethylsilane (2 mL, 16 mmol) was added dropwise to lithium borohydride (2M in tetrahydrofuran, 4 mL, 8 mmol). A solution of 3-fluoro-4-(trifluoromethyl)phenylacetonitrile (312 mg, 4 mmol) in tetrahydrofuran (2 mL) was then added at 0° C. and the mixture was allowed to stir for 24 hours, whilst warming to room temperature. The mixture was then diluted with methanol (20 mL) and concentrated in vacuo. The residue was taken up in 20% potassium hydroxide solution (20 mL), extracted with dichloromethane (3×20 mL) and the combined organic solution was dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography using an Isolute® SCX-2 cartridge, eluting with methanol followed by 1M ammonia in methanol, to give an oily residue. The oil was triturated with diethyl ether to afford the title compound in 59% yield, 485 mg. H NMR (400 MHz, CDCl3) δ: 7.53 (1H, m), 7.08 (2H, m), 3.02 (2H, t) 2.82 (2H, t) ppm; LRMS APCI m/z 208 [M+H]+

1. concentrationconcentrated in vacuo
2. extractionextracted with dichloromethane (3×20 mL)
3. dry with materialthe combined organic solution was dried over magnesium sulfate
4. concentrationconcentrated in vacuo
5. customThe residue was purified by column chromatography
6. washeluting with methanol
7. customto give an oily residue
8. customThe oil was triturated with diethyl ether

ORDレコード

ord-cf3ddf4829644a53b7ae71a5c55920eb

出典データセット

uspto-grants-2009_12

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07629358B2