Tetrahydrofuran → 2-Phenyl-1-(2-phenyl-[1,3]-dithian-2-yl)-ethanol
反応式
[C:1]1([CH:7]2[S:12][CH2:11][CH2:10][CH2:9][S:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:13]([Li])[CH2:14][CH2:15][CH3:16].[CH2:18]1[CH2:22][O:21][CH2:20][CH2:19]1>>[C:18]1([CH2:19][CH:20]([C:7]2([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[S:8][CH2:9][CH2:10][CH2:11][S:12]2)[OH:21])[CH:22]=[CH:16][CH:15]=[CH:14][CH:13]=1参加物
反応条件
- 温度
- -30 °C
実験手順
To a solution of 2-phenyl-[1,3]-dithiane (65) (4.0 g, 20.4 mmol) in THF at −30° C. was added a 1.6 M solution of n-butyllithium in THF (15.3 mL, 24.4 mmol). After stirring for 30 minutes at −30° C., a solution of phenylacetylaldehyde (2.45 g, 20.4 mmol) in tetrahydrofuran was added dropwise at −30° C. The resulting reaction mixture was stirred for another hour at 0° C. The reaction was quenched with saturated NH4Cl solution and extracted with ethyl acetate. The combined organic extracts were washed with saturated NH4Cl solution, brine and dried over Na2SO4. After filtrating and concentrating, the crude product was purified by flash chromatography on silica gel, (25% ethyl acetate in hexanes), to afford 2.63 g (71%) of the title compound (66). 1H NMR (CDCl3, 400 MHz): δ 1.97 (m, 2H), 2.23 (dd, J=4.0, 1.2 Hz, 1H), 2.43 (dd, J=13.6, 10.2 Hz, 1H), 2.77 (m, 4H), 3.02 (d, J=13.6 Hz, 1H), 4.07 (m, 1H), 7.44-7.13 (m, 8H), 8.02 (dd, J=8.4, 1.4 Hz, 2H).
後処理
- customThe resulting reaction mixture
- stirringwas stirred for another hour at 0° C
- customThe reaction was quenched with saturated NH4Cl solution
- extractionextracted with ethyl acetate
- washThe combined organic extracts were washed with saturated NH4Cl solution, brine
- dry with materialdried over Na2SO4
- filtrationAfter filtrating
- concentrationconcentrating
- customthe crude product was purified by flash chromatography on silica gel, (25% ethyl acetate in hexanes),
出典と根拠
- ORDレコード
- ord-4af3009cbae14543a6769b28f3b7dfd5
- 出典データセット
- uspto-grants-2005_12
- 特許番号
- US06972341B2
反応ノート
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