Ethanol → Ethyl 4-bromopyrrole-2-carboxylate

HRID 74484

反応式

HRID 74484 の反応式
[CH2:1]([O:3][C:4]([C:6]1[NH:7][CH:8]=[CH:9][CH:10]=1)=[O:5])[CH3:2].[Br:11]Br.C(O)C.[O-]CC.[Na+]>C(Cl)(Cl)(Cl)Cl>[CH2:1]([O:3][C:4]([C:6]1[NH:7][CH:8]=[C:9]([Br:11])[CH:10]=1)=[O:5])[CH3:2]

参加物

6

反応条件

温度
25 °C

実験手順

1H-Pyrrole-2-carboxylic acid ethyl ester (10 g) was dissolved in carbon tetrachloride (50 ml). A carbon tetrachloride solution (50 ml) of bromine was added dropwise thereto on ice over 30 minutes. The reaction mixture was stirred at 25° C. for one hour. The suspension of reaction mixture was added dropwise to an ethanol solution (100 ml) of 10% sodium ethoxide on ice over 20 minutes. The solvent was concentrated under reduced pressure. The resulting residue was diluted with ethyl acetate (40 ml) and water (20 ml). The organic layer was washed with an aqueous solution saturated with sodium chloride (10 ml), and then concentrated. The residue obtained by concentration under reduced pressure was purified by silica gel column chromatography (hexane/ethyl acetate). Thus, a brown solid was obtained (10 g, 99%).

後処理

  1. additionThe suspension of reaction mixture
  2. concentrationThe solvent was concentrated under reduced pressure
  3. additionThe resulting residue was diluted with ethyl acetate (40 ml) and water (20 ml)
  4. washThe organic layer was washed with an aqueous solution saturated with sodium chloride (10 ml)
  5. concentrationconcentrated
  6. customThe residue obtained by concentration under reduced pressure
  7. customwas purified by silica gel column chromatography (hexane/ethyl acetate)
  8. customThus, a brown solid was obtained (10 g, 99%)

出典と根拠

ORDレコード
ord-fd68bc68f7e64f2d868a563444a0b180
出典データセット
uspto-grants-2014_09
特許番号
US08829199B2

関連ノート

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