反応式
N[C@H:2]([CH2:6][CH2:7][C:8]([F:11])([F:10])[F:9])[C:3]([OH:5])=[O:4].[OH:12]S(O)(=O)=O.N([O-])=O.[Na+]>O.CCOCC>[F:9][C:8]([F:11])([F:10])[CH2:7][CH2:6][C@@H:2]([OH:12])[C:3]([OH:5])=[O:4]参加物
反応条件
- 温度
- 0 °C
実験手順
To a cool (0° C.), stirred solution of (2R)-2-amino-5,5,5-trifluoropentanoic acid (4.09 g, 23.90 mmol) (U.S. Pat. No. 2009/0111858 A1) and H2SO4 (2.8 mL, 52.5 mmol) in water (95 mL) was added a solution of sodium nitrite (9.89 g, 143 mmol) in water (30 mL) dropwise via addition funnel over 60 min. The reaction mixture was allowed to slowly warm to room temperature and stirred overnight. The reaction mixture was diluted with Et2O, the aqueous phase was separated and extracted with Et2O (3×). The combined organics were dried (Na2SO4), filtered and concentrated under reduced pressure to provide Intermediate S-3A (4.1551 g, >99%) as an amber oil: 1H NMR (400 MHz, CDCl3) δ ppm 4.33 (1H, dd, J=8.03, 4.27 Hz), 2.09-2.42 (3H, m), 1.88-2.02 (1H, m).
後処理
- additiondropwise via addition funnel over 60 min
- temperatureto slowly warm to room temperature
- customthe aqueous phase was separated
- extractionextracted with Et2O (3×)
- dry with materialThe combined organics were dried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customto provide Intermediate S-3A (4.1551 g, >99%) as an amber oil
出典と根拠
- ORDレコード
- ord-84d73495319e4ff8ae8cadf41ffc8603
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09187434B2
関連ノート
読み込み中…