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Acetyl chloride → HCID 4155152、化合物

HRID 703894
ノート
印刷プレビュー

反応式

HRID 703894 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([Br:14])=[CH:10][CH:9]=2)=[CH:4][CH:3]=1.[C:15](Cl)(=[O:17])[CH3:16]>N1C=CC=CC=1>[Br:14][C:11]1[CH:12]=[CH:13][C:8]([C:5]2[CH:4]=[CH:3][C:2]([NH:1][C:15](=[O:17])[CH3:16])=[CH:7][CH:6]=2)=[CH:9][CH:10]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6367Acetyl chlorideHCID 2795744'-Bromo-[1,1'-biphenyl]-4-amine

生成物 1

HCID 4155152HCID 4155152、化合物収率 91.2%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

[I] A solution prepared by dissolving 0.75 g of 4-amino-4'-bromobiphenyl in 10 ml of pyridine, was cooled with ice, and 1.0 g of acetyl chloride was dropwise added thereto. The mixture was stirred over a period of 30 minutes. After the completion of the reaction, the reaction solution was extracted with ethyl acetate and water. The organic layer was washed with dilute hydrochloric acid and further with a saturated sodium chloride aqueous solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain 0.8 g of N-(4'-bromo-4-biphenylyl)acetamide as colorless crystals.

後処理

  1. custom[I] A solution prepared
  2. additionwas dropwise added
  3. customAfter the completion of the reaction
  4. extractionthe reaction solution was extracted with ethyl acetate and water
  5. washThe organic layer was washed with dilute hydrochloric acid and further with a saturated sodium chloride aqueous solution
  6. dry with materialdried over anhydrous sodium sulfate
  7. distillationThe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-d48f63ba40444728a8a1c53c7c3e3995
出典データセット
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04985449

反応ノート

読み込み中…

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