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Dimethylformamide → HCID 19102568、化合物

HRID 1198546
ノート
印刷プレビュー

反応式

HRID 1198546 の反応式
[H-].[Na+].C[C:4](P(OC)(O)=O)([C:6]([O-:8])=[O:7])[CH3:5].[CH2:14]([O:21][C:22]1[C:30]2[NH:29][CH:28]=[CH:27][C:26]=2[C:25](C=O)=[CH:24][CH:23]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[CH3:33]N(C)C=O>O1CCCC1>[CH2:14]([O:21][C:22]1[CH:23]=[CH:24][C:25](/[CH:5]=[CH:4]/[C:6]([O:8][CH3:33])=[O:7])=[C:26]2[C:30]=1[NH:29][CH:28]=[CH:27]2)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6228DimethylformamideHCID 24758Sodium hydrideHCID 132434867-(Benzyloxy)-1H-indole-4-carbaldehydeHCID 53413272Trimethylphosphonoacetate

生成物 1

HCID 19102568HCID 19102568、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

60% Sodium hydride dispersion (0.10 g, 2.5 mmol) was added to a stirred solution of trimethylphosphonoacetate (0.41 ml, 2.5 mmol) in tetrahydrofuran (10 ml). The pale suspension was stirred for 1 hour at room temperature then a solution of 7-benzyloxyindole-4-carboxaldehyde (0.63 g, 2.5 mmol) in tetrahydrofuran (5 ml) was added followed by dimethylformamide (5 ml) to give a clear solution. The solution was stirred for 1 hour at room temperature then evaporated under high vacuum. The residue in ethyl acetate was washed with dilute hydrochloric acid dried and concentrated to give pale solid.

後処理

  1. customto give a clear solution
  2. stirringThe solution was stirred for 1 hour at room temperature
  3. customthen evaporated under high vacuum
  4. washThe residue in ethyl acetate was washed with dilute hydrochloric acid
  5. customdried
  6. concentrationconcentrated
  7. customto give pale solid

出典と根拠

ORDレコード
ord-a22637df0ac647a783a8837d65e55557
出典データセット
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05281593

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート