Water → 104501-20-4

HRID 2291931ノート

反応式

HRID 2291931 の反応式
[NH:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([O:8][CH3:9])=[O:7].[H-].[Na+].[CH2:12](Br)[C:13]#[CH:14].O>O1CCCC1>[CH2:14]([N:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]([O:8][CH3:9])=[O:7])[C:13]#[CH:12]

参加物

6

反応物 4

HCID 962WaterHCID 7842Propargyl bromide2 回HCID 24758Sodium hydrideHCID 136930Methyl pyrrole-2-carboxylate

生成物 1

HCID 21278433104501-20-4

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
20 °C

実験手順

3.302 g of methyl 1H-pyrrole-2-carboxylate were dissolved in 40 ml of tetrahydrofuran and then, at 0° C., 1.422 g of sodium hydride in suspension at 50% in vaseline oil were added. The mixture stirred for 1 hour at 20° C. and a solution of 2 ml of propargyl bromide in 10 ml of tetrahydrofuran was introduced dropwise. The mixture was stirred for 1 hour at 50° C. and after having added 5 ml of propargyl bromide, the reaction mixture was poured into water. The mixture was extracted with methylene chloride and the extracts were concentrated to dryness by distilling under reduced pressure. The residue was chromatographed over silica and eluted with a mixture of hexane and ethyl acetate (9-1) to obtain 2.993 g of methyl 1-(2-propynyl)-1H-pyrrol-2-carboxylate.

後処理

  1. stirringThe mixture was stirred for 1 hour at 50° C.
  2. extractionThe mixture was extracted with methylene chloride
  3. concentrationthe extracts were concentrated to dryness
  4. distillationby distilling under reduced pressure
  5. customThe residue was chromatographed over silica
  6. washeluted with a mixture of hexane and ethyl acetate (9-1)

出典と根拠

ORDレコード
ord-d8c34933890f44f983951c1e7fc3c49b
出典データセット
uspto-grants-1989_01
特許番号
US04798901

反応ノート

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