反応式
[F:1][C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8][CH2:9]Cl)=[O:7])=[CH:4][CH:3]=1.[Na+].[I-:14]>CC(C)=O>[F:1][C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8][CH2:9][I:14])=[O:7])=[CH:4][CH:3]=1参加物
4
実験手順
To a solution of chloromethyl 4-fluorobenzoate (3.0g, 15.9 mmol) in 50 mL of dry acetone, NaI (4.8 g, 31.8 mmol) was added and the mixture was stirred overnight. The solvent was removed and Et2O (150 mL) was added to the solid residues and the mixture was stirred for 10 min. After filtration the filtrate was washed with 5% NaHSO3 (aq) (2×25 mL) followed by brine. The organic solution was concentrated by rotary evaporation and purified by silica gel chromatography to give a light yellow oil. Yield 3.7 g (85%). 1H NMR (300 MHz, CDCl3): δ 6.16 (s, 2H), 7.17 (m, 2H), 8.08 (m, 2H).
後処理
- customThe solvent was removed
- additionEt2O (150 mL) was added to the solid residues
- stirringthe mixture was stirred for 10 min
- filtrationAfter filtration the filtrate
- washwas washed with 5% NaHSO3 (aq) (2×25 mL)
- concentrationThe organic solution was concentrated by rotary evaporation
- custompurified by silica gel chromatography
- customto give a light yellow oil
出典と根拠
- ORDレコード
- ord-3a7da02939a042cb873473416ffb7bfe
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08841257B2
関連ノート
読み込み中…