反応 #2348122

ord-94d45aab2d0c4d6e88a436fb64fbf189

反応方程式

[Na+].[OH-]
NaOH
Sc1ccccc1
Thiophenol
C(=C\c1ccccc1)/c1ccccc1
trans-stilbene
CN1CCCC1=O
NMP
O=C([O-])[O-].[K+].[K+]
K2CO3
Oc1ccc(/C=C/c2ccc(O)nc2)cc1
5-[(E)-2-(4-hydroxyphenyl)-vinyl]-pyridin-2-ol
収率 69.0%

反応条件

温度
195°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The cooled reaction mixture
  2. 2
    抽出the neutral components were extracted with ether (3×50 mL)
  3. 3
    抽出extracted with ether (2×50 mL)
  4. 4
    その他The solid was isolated by filtration
  5. 5
    洗浄washed with water (100 mL), ethyl acetate (50 mL) and ether (30 mL)
  6. 6
    その他air-dried

実験手順

The trans-stilbene (1.17 g, 4.85 mmol) was dissolved in dry NMP (12 mL). Thiophenol (1.07 g, 9.7 mmol) was then added to the above solution, followed by addition of K2CO3 (67 mg, 0.48 mmol). The resulting mixture was heated for 8 hours at 195° C. under nitrogen. The cooled reaction mixture was made alkaline with 1 N NaOH (pH=10), and the neutral components were extracted with ether (3×50 mL). The aqueous layer was acidified to pH=4 with 1 N HCl and stirred at room temperature for 30 minutes, and extracted with ether (2×50 mL). Then pH was adjusted to pH=8 with saturated NaHCO3. The solid was isolated by filtration, washed with water (100 mL), ethyl acetate (50 mL) and ether (30 mL), and air-dried to yield 5-[(E)-2-(4-hydroxyphenyl)-vinyl]-pyridin-2-ol (715 mg, 69%). MS (ES) m/z: 214.08 (M+1); 13C-NMR (DMSO-d6): δ 162.42, 157.50, 138.21, 134.07, 129.04, 127.92, 125.67, 121.59, 121.03, 116.89, and 116.18.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07846915B2uspto-grants-2010_12