Benzamide → 4-(Chloromethyl)-2-phenyl-1,3-oxazole

HRID 404621

反応式

HRID 404621 の反応式
[C:1]([NH2:9])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:10][CH2:11][C:12](=O)[CH2:13]Cl>>[Cl:10][CH2:11][C:12]1[N:9]=[C:1]([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[O:8][CH:13]=1

参加物

3

反応条件

温度
130 °C

実験手順

A mixture of benzamide (0.80 g, 6.60 mmol) and 1,3-dichloropropan-2-one (1.01 g, 7.92 mmol) was heated to 130° C. for 1 hour under nitrogen atmosphere. The crude was purified by crystallization from acetonitrile (25 ml): the suspension was heated to reflux and a brown solution with a white insoluble solid was obtained. It was filtered and the solution was cooled to room temperature. A precipitate formed and the suspension was filtered on a buckner funnel washing with acetonitrile (8 ml). The solid was recovered from the filter, dissolved in EtOAc (20 ml) and washed with 1N NaHCO3 (15 ml). The organic phase was dried (Na2SO4) and evaporated to give 4-(chloromethyl)-2-phenyloxazole (315 mg, 25% yield) as a pale brown solid.

後処理

  1. customThe crude was purified by crystallization from acetonitrile (25 ml)
  2. temperaturethe suspension was heated
  3. temperatureto reflux
  4. customa brown solution with a white insoluble solid was obtained
  5. filtrationIt was filtered
  6. temperaturethe solution was cooled to room temperature
  7. customA precipitate formed
  8. filtrationthe suspension was filtered on a buckner funnel
  9. washwashing with acetonitrile (8 ml)
  10. customThe solid was recovered from the filter
  11. dissolutiondissolved in EtOAc (20 ml)
  12. washwashed with 1N NaHCO3 (15 ml)
  13. dry with materialThe organic phase was dried (Na2SO4)
  14. customevaporated

出典と根拠

ORDレコード
ord-992a7a090fe04bf0bc9a3cf3d87f59c2
出典データセット
uspto-grants-2014_06
特許番号
US08748613B2

関連ノート

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