2,6-Lutidine → 3-Fluoropropyl trifluoromethanesulfonate
反応式
N1C(C)=CC=CC=1C.S([O:16][S:17]([C:20]([F:23])([F:22])[F:21])(=[O:19])=[O:18])(C(F)(F)F)(=O)=O.[F:24][CH2:25][CH2:26][CH2:27]O>C(Cl)Cl>[F:24][CH2:25][CH2:26][CH2:27][O:16][S:17]([C:20]([F:21])([F:22])[F:23])(=[O:18])=[O:19]参加物
実験手順
To a cold (−25° C.), stirred solution of 2,6-Lutidine (4.60 mL, 39.5 mmoL) in DCM (30 mL) was added triflic anhydride (6.00 mL, 35.5 mmoL) over 3 min. Then 3-fluoropropane-1-ol (1.61 g, 20.6 mmoL) was added. The reaction mixture was warmed to room temperature for 2.5 h. The reaction mixture was then concentrated to half its volume and purified by flash chromatography (Teledyne ISCO CombiFlash, isocratic DCM, REDISEP® SiO2 120 g, detecting at 254 nM, and monitoring at 220 nM). Concentration of the appropriate fractions provided Intermediate S-4A (2.92 g, 67.4%). 1H NMR (400 MHz, chloroform-d) δ ppm 4.69 (2H, t, J=6.16 Hz), 4.65 (1H, t, J=5.50 Hz), 4.54 (1H, t, J=5.61 Hz), 2.25 (1H, dt, J=11.39, 5.86 Hz), 2.19 (1H, dt, J=11.44, 5.94 Hz)
後処理
- concentrationThe reaction mixture was then concentrated to half its volume
- custompurified by flash chromatography (Teledyne ISCO CombiFlash, isocratic DCM, REDISEP® SiO2 120 g, detecting at 254 nM, and monitoring at 220 nM)
- customConcentration of the appropriate fractions provided Intermediate S-4A (2.92 g, 67.4%)
出典と根拠
- ORDレコード
- ord-5cc680f4e9cc44fa84c60879d1b8e6f5
- 出典データセット
- uspto-grants-2016_02
- 特許番号
- US09249157B2
反応ノート
読み込み中…