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Phloroglucinol → HCID 14438698、化合物

HRID 2051319
ノート
印刷プレビュー

反応式

HRID 2051319 の反応式
[C:1]1([CH:9]=[C:7]([OH:8])[CH:6]=[C:4]([OH:5])[CH:3]=1)[OH:2].N1C=CC=CC=1.Cl[C:17]([C:19]1[C:31]2[C:30]3[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=3)[C:24](=[C:32]([C:35]#[N:36])[C:33]#[N:34])[C:23]=2[CH:22]=[CH:21][CH:20]=1)=[O:18]>ClCCl>[C:35]([C:32]([C:33]#[N:34])=[C:24]1[C:23]2[CH:22]=[CH:21][CH:20]=[C:19]([C:17]([O:2][C:1]3[CH:9]=[C:7]([OH:8])[CH:6]=[C:4]([OH:5])[CH:3]=3)=[O:18])[C:31]=2[C:30]2[C:25]1=[CH:26][CH:27]=[CH:28][CH:29]=2)#[N:36]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 359PhloroglucinolHCID 1049PyridineHCID 198332559-(Dicyanomethylidene)-9H-fluorene-4-carbonyl chloride

生成物 1

HCID 14438698HCID 14438698、化合物収率 58.3%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A solution of 30.0 grams of phloroglucinol and 70 milliliters of pyridine in 300 milliliters of dichloromethane was stirred at room temperature under a nitrogen atmosphere. Thereafter, a solution of 8.0 grams of (4-chloroformyl-9-fluorenylidene)malononitrile in 400 milliliters of dichloromethane was added thereto over a period of 1 hour. After addition, the reaction mixture was further stirred for another hour. The mixture was washed three times dilute aqueous HCl solution, twice with dilute aqueous NaHCO3 solution, and once with water. The solution was dried, filtered, and evaporated under reduced pressure to give the crude product. Recrystallization from methanol afforded 6.1 grams of (b), mp., 255.5° to 257° C.

後処理

  1. additionAfter addition
  2. washThe mixture was washed three times dilute aqueous HCl solution
  3. customThe solution was dried
  4. filtrationfiltered
  5. customevaporated under reduced pressure
  6. customto give the crude product
  7. customRecrystallization from methanol

出典と根拠

ORDレコード
ord-d0d05c1f69a74573bff354a63ad9e2ed
出典データセット
uspto-grants-1991_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05017645

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