反応 #2254203

ord-6e04ebacc15b4e438e419dc49931b4f5

反応方程式

O
H2O
[K+].[OH-]
KOH
COC(=O)C(C#N)C1(c2ccc(F)cc2)CCOCC1
methyl 2-cyano-2-[4-(4-fluorophenyl)oxan-4-yl]acetate
N#CCC1(c2ccc(F)cc2)CCOCC1
2-[4-(4-fluorophenyl)oxan-4-yl]acetonitrile

反応条件

温度
120°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooled
  2. 2
    抽出the product extracted with Et2O (3×50 ml)
  3. 3
    洗浄washed with H2O (50 ml)
  4. 4
    その他dried over NA2SO4
  5. 5
    ろ過filtered
  6. 6
    濃縮concentrated
  7. 7
    その他Purified by normal phase SiO2 chromatography (5 to 40% EtOAc/hexanes)

実験手順

To a pre-dissolved solution of KOH (441 mg, 7.87 mmol) in ethylene glycol (20 ml) was added methyl 2-cyano-2-[4-(4-fluorophenyl)oxan-4-yl]acetate (1.09 g, 3.93 mmol). The mixture was heated to 120° C. for 3 h, and then cooled. H2O was added (50 ml), the product extracted with Et2O (3×50 ml), washed with H2O (50 ml), dried over NA2SO4, filtered and concentrated. Purified by normal phase SiO2 chromatography (5 to 40% EtOAc/hexanes) to give 2-[4-(4-fluorophenyl)oxan-4-yl]acetonitrile as a colorless oil (450 mg, 78%, m/z: 219.1 [M+H]+ observed).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09044469B2uspto-grants-2015_06