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
- customThe crude was purified by crystallization from acetonitrile (25 ml)
- temperaturethe suspension was heated
- temperatureto reflux
- customa brown solution with a white insoluble solid was obtained
- filtrationIt was filtered
- temperaturethe solution was cooled to room temperature
- customA precipitate formed
- filtrationthe suspension was filtered on a buckner funnel
- washwashing with acetonitrile (8 ml)
- customThe solid was recovered from the filter
- dissolutiondissolved in EtOAc (20 ml)
- washwashed with 1N NaHCO3 (15 ml)
- dry with materialThe organic phase was dried (Na2SO4)
- 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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