Potassium Carbonate → Ethyl 2-(6-acetyl-4-chloro-3-fluoro-2-iodophenoxy)propanoate
反応式
[Cl:1][C:2]1[C:3]([F:13])=[C:4]([I:12])[C:5]([OH:11])=[C:6]([C:8](=[O:10])[CH3:9])[CH:7]=1.C(=O)([O-])[O-].[K+].[K+].Br[CH:21]([CH3:27])[C:22]([O:24][CH2:25][CH3:26])=[O:23]>CN(C)C=O.O.C(OCC)(=O)C>[C:8]([C:6]1[C:5]([O:11][CH:21]([CH3:27])[C:22]([O:24][CH2:25][CH3:26])=[O:23])=[C:4]([I:12])[C:3]([F:13])=[C:2]([Cl:1])[CH:7]=1)(=[O:10])[CH3:9]参加物
反応条件
- 温度
- 60 °C
実験手順
A solution of 1-(5-chloro-4-fluoro-2-hydroxy-3-iodophenyl)ethanone (5.00 g, 15.9 mmol) in N,N-dimethylformamide (80.0 mL) was treated with potassium carbonate (4.39 g, 31.8 mmol), followed by ethyl 2-bromopropanoate (2.48 mL, 19.1 mmol), and then stirred at 60° C. for 3 h. The reaction was stirred overnight at 60° C., and then worked up per the procedure below. The reaction was then re-submitted to the reaction conditions and stirred at 90° C. for 4 h. The reaction mixture was diluted with water and ethyl acetate. The organic layer was separated and washed with brine, dried over magnesium sulfate, filtered, and concentrated to give a crude residue. Purification by flash column chromatography (100% hexanes to 10% EtOAc/hexanes) gave the desired product (3.66 g, 56%) as a mixture of enantiomers. LCMS calculated for C13H14ClFIO4 (M+H)+: m/z=415.0; found: 414.9.
後処理
- stirringThe reaction was stirred overnight at 60° C.
- customre-submitted to the reaction conditions
- stirringstirred at 90° C. for 4 h
- customThe organic layer was separated
- washwashed with brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customto give a crude residue
- customPurification by flash column chromatography (100% hexanes to 10% EtOAc/hexanes)
出典と根拠
- ORDレコード
- ord-6673da53b50647f48876eaafdce51dff
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09309251B2
反応ノート
読み込み中…