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Dimethylformamide → HCID 19935434、化合物

HRID 373556
ノート
印刷プレビュー

反応式

HRID 373556 の反応式
P(Cl)(Cl)(Cl)=O.[CH3:6][N:7]1[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=2[CH2:11][CH2:10][CH2:9][CH2:8]1.[OH-].[Na+].CN(C)[CH:22]=[O:23]>>[CH3:6][N:7]1[C:13]2[CH:14]=[CH:15][C:16]([CH:22]=[O:23])=[CH:17][C:12]=2[CH2:11][CH2:10][CH2:9][CH2:8]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 6228DimethylformamideHCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 132624261-Methyl-2,3,4,5-tetrahydro-1H-1-benzazepine

生成物 1

HCID 19935434HCID 19935434、化合物

反応条件

温度
70 °C

実験手順

The starting material was prepared as follows: A. 45 ml of dimethylformamide were treated under an argon atmosphere with 16.2 ml of phosphorus oxychloride. After the reaction had faded away, 7.30 g of 2,3,4,5-tetrahydro-1-methyl-1H-1-benzazepine were added and the reaction mixture was stirred at 70° C. for 5 hours. Thereafter, the mixture was poured on to ice, made alkaline with sodium hydroxide solution, extracted with ether, washed with water, dried and evaporated. Chromatorgraphy on silica gel (petroleum ether/ethyl acetate (87:13)) yielded 4.38 g of 2,3,4,5-tetrahydro-1-methyl-1H-1-benzazepine-7-carboxaldehyde.

後処理

  1. customThe starting material was prepared
  2. additionThereafter, the mixture was poured on to ice
  3. extractionextracted with ether
  4. washwashed with water
  5. customdried
  6. customevaporated

出典と根拠

ORDレコード
ord-ac5cbf8d5de240d386e8882c0e802b6b
出典データセット
uspto-grants-1992_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05164387

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート