Ethyl bromoacetate → ethyl 2-(1H-1,3-benzodiazol-2-ylsulfanyl)acetate

HRID 2059957

反応式

HRID 2059957 の反応式
[NH:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[NH:3][C:2]1=[S:10].C(=O)([O-])[O-].[K+].[K+].Br[CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20]>C(O)C>[NH:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[S:10][CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20]

参加物

5

反応物 3

HCID 7748Ethyl bromoacetateHCID 11430Potassium CarbonateHCID 7070352-Mercaptobenzimidazole

生成物 1

HCID 21564ethyl 2-(1H-1,3-benzodiazol-2-ylsulfanyl)acetate収率 30,947.1%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a stirred solution of 1H-benzo[d]imidazole-2(3H)-thione (20.0 g, 0.13 mol, 1.0 eq.) in anhydrous ethanol (500 mL) at room temperature, was added potassium carbonate (9.25 g, 0.07 mol, 0.5 eq.) and ethyl bromoacetate (26.7 g, 0.16 mmol, 1.2 eq.). The reaction was heated to reflux and stirred at that temperature for 6 hours. The solvent was removed in vacuo and water (200 mL) was added. The aqueous phase was extracted with dichloromethane (3×100 mL), and the combined organic extracts were washed with water (200 mL) and brine (200 mL). The organic phase was dried over magnesium sulfate and concentrated in vacuo to give a colorless oil which solidified on standing. Purification by flash chromatography (CHCl3→10% MeOH:90% CHCl3) gave 4a as a white solid (11.7 g, 37%).

後処理

  1. temperatureThe reaction was heated
  2. temperatureto reflux
  3. customThe solvent was removed in vacuo and water (200 mL)
  4. additionwas added
  5. extractionThe aqueous phase was extracted with dichloromethane (3×100 mL)
  6. washthe combined organic extracts were washed with water (200 mL) and brine (200 mL)
  7. dry with materialThe organic phase was dried over magnesium sulfate
  8. concentrationconcentrated in vacuo
  9. customto give a colorless oil which
  10. customPurification by flash chromatography (CHCl3→10% MeOH:90% CHCl3)

出典と根拠

ORDレコード
ord-fd220d09049246eba6a85a82436efdbe
出典データセット
uspto-grants-2012_10
特許番号
US08278327B2

関連ノート

読み込み中…