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Hydrochloric Acid → N-(4-t-butylphenyl)perylene-3,4-dicarboximide

HRID 266605
ノート
印刷プレビュー

反応式

HRID 266605 の反応式
[CH:1]1[C:18]2=[C:19]3[C:8]([C:9]4[C:20]5[C:13](=[CH:14][CH:15]=[CH:16][C:17]2=5)[CH:12]=[CH:11][CH:10]=4)=[CH:7][CH:6]=[C:5]2[C:21]([O:23][C:24](=O)[C:3](=[C:4]23)[CH:2]=1)=[O:22].[C:26]([C:30]1[CH:36]=[CH:35][C:33]([NH2:34])=[CH:32][CH:31]=1)([CH3:29])([CH3:28])[CH3:27].N1C=CN=C1.Cl>O.O.C([O-])(=O)C.[Zn+2].C([O-])(=O)C.C(O)C>[C:26]([C:30]1[CH:31]=[CH:32][C:33]([N:34]2[C:21](=[O:22])[C:5]3[C:4]4[C:19]5[C:8](=[CH:7][CH:6]=3)[C:9]3[C:20]6[C:13]([CH:12]=[CH:11][CH:10]=3)=[CH:14][CH:15]=[CH:16][C:17]=6[C:18]=5[CH:1]=[CH:2][C:3]=4[C:24]2=[O:23])=[CH:35][CH:36]=1)([CH3:29])([CH3:27])[CH3:28]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 795ImidazoleHCID 698614-Tert-ButylanilineHCID 11759069Perylene-3,4-dicarboxylic anhydride

生成物 1

HCID 19033222N-(4-t-butylphenyl)perylene-3,4-dicarboximide収率 81.3%

試薬・触媒・溶媒 2

HCID 2724192
Zinc acetate (USP)
触媒
HCID 702Ethanol溶媒2 回

実験手順

0.70 g (2.17 mmol) of perylene-3,4-dicarboxylic anhydride is mixed with 0.49 g (3.28 mmol) of 4-t-butylaniline, 3.00 g of imidazole and 0.10 g of zinc acetate dihydrate and the mixture is heated at 140°-150° C. for 5 h. While still hot, the mixture is treated with 100 ml of ethanol, and then 200 ml of 10% hydrochloric acid are added. The red suspension is heated until all the ethanol has evaporated, and the product is then filtered off with suction. The red-brown residue is boiled in 10% potassium carbonate solution, the solid residue is filtered off with suction while hot and rinsed several times with hot dist. water. The red residue is dried in a drying cabinet at 120° C. and then recrystallized by extraction with a toluene/methanol mixture to give 0.80 g (81%) of red N-(4-t-butylphenyl)perylene-3,4-dicarboximide which shows a red solid fluorescence. M.p. >330° C. Rf (CHCl3 /silica gel)=0.35.

後処理

  1. temperaturethe mixture is heated at 140°-150° C. for 5 h
  2. customhas evaporated
  3. filtrationthe product is then filtered off with suction
  4. filtrationthe solid residue is filtered off with suction while hot and
  5. washrinsed several times with hot dist
  6. customThe red residue is dried in a drying cabinet at 120° C.
  7. customrecrystallized by extraction with a toluene/methanol mixture

出典と根拠

ORDレコード
ord-16dd334854764a0590178515dbeeb052
出典データセット
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05650513

反応ノート

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