ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Diethylamine → 4-(Diethylamino)benzonitrile

HRID 449
ノート
印刷プレビュー

反応式

HRID 449 の反応式
CCNCC.N#Cc1ccc(Br)cc1>CC#N.CC(=O)O.CC(=O)O.CC(C)c1cc(C(C)C)c(-c2ccccc2P(C2CCCCC2)C2CCCCC2)c(C(C)C)c1.O=C([O-])[O-].[K+].[K+].[Pd]>CCN(CC)c1ccc(C#N)cc1
参加物反応条件実験手順出典と根拠反応ノート

参加物

7

反応物 2

HCID 8021DiethylamineHCID 12162Benzonitrile, 4-bromo-

生成物 1

HCID 761344-(Diethylamino)benzonitrile収率 39.17%

試薬・触媒・溶媒 4

HCID 11430Potassium Carbonate試薬HCID 4144353Palladium (II) acetate触媒HCID 11155794
2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl
触媒
HCID 6342Acetonitrile溶媒

反応条件

温度
160 °C

実験手順

4-Bromobenzonitrile (2.000 g, 10.99 mmol), diethylamine (3.41 mL, 32.96 mmol) and POTASSIUM CARBONATE (4.56 g, 32.96 mmol) were mixed in dry acetonitrile (10 mL) under argon in a microwave vial. The vial was sealed and heated with microvawes for 60 minutes at 160°C. Added diethylamine (3.41 mL, 32.96 mmol) and heated at 160°C for 3 hours. Added Palladium(II) acetate (0.123 g, 0.55 mmol) and 2-(Dicyclohexylphosphino)-2',4',6'-tri-i- propyl-1,1'-biphenyl (0.524 g, 1.10 mmol), purged with argon for 5 minutes and heated in an oil bath at 100°C for 24 hours. The reaction was cooled to rt and partitioned between EtOAc (100 mL) and saturated aqueous NaHCO3 (40 mL). The layers were separated and the aqueous phase extracted with EtOAc (100 mL). The organics were combined, dried (Na2SO4), filtered and concentrated. Purification by flash chromatography on silica gel gave 4-(diethylamino)benzonitrile (0.750 g, 39.2 %)

出典と根拠

ORDレコード
ord-45a7a9da12934ab5ab153542a819eb23
出典データセット
750 AstraZeneca ELN dataset
元リンク
出典を表示

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出典と根拠反応ノート