Nitrogen oxide (N2O4) → 3-(4-Carboxyphenyl)-2-nitronaphtho-[1,2-b]furan

HRID 224309

反応式

HRID 224309 の反応式
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[C:11]3[CH:22]=[CH:21][C:20]4[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=4)[C:12]=3[O:13][CH:14]=2)=[CH:6][CH:5]=1)([OH:3])=[O:2].[N+:23]([O-:28])([N+]([O-])=O)=[O:24]>C(Cl)(Cl)Cl>[C:1]([C:4]1[CH:5]=[CH:6][C:7]([C:10]2[C:11]3[CH:22]=[CH:21][C:20]4[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=4)[C:12]=3[O:13][C:14]=2[N+:23]([O-:28])=[O:24])=[CH:8][CH:9]=1)([OH:3])=[O:2]

参加物

4

反応物 2

HCID 25352Nitrogen oxide (N2O4)HCID 15571610HCID 15571610、化合物

生成物 1

HCID 129404983-(4-Carboxyphenyl)-2-nitronaphtho-[1,2-b]furan

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

反応条件

温度
20 °C

実験手順

To a mixture of 4.0 g. of the product of step A in 250 ml. of chloroform is added 4.0 g. of dinitrogen tetraoxide. The mixture is stirred at about 20° C. for 20 hours. The mixture is filtered, and the solid obtained is recrystallized from a mixture of N,N-dimethylformamide and water to provide yellow crystals of 3-(4-carboxyphenyl)-2-nitronaphtho-[1,2-b]furan, m.p. greater than 300° C.

後処理

  1. additionTo a mixture of 4.0 g
  2. filtrationThe mixture is filtered
  3. customthe solid obtained
  4. customis recrystallized from a mixture of N,N-dimethylformamide and water

出典と根拠

ORDレコード
ord-e836115ea43f4f0aac8213eac82c4454
出典データセット
uspto-grants-1980_11
特許番号
US04231965

関連ノート

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