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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
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Water → HCID 20155091、化合物

HRID 364920
ノート
印刷プレビュー

反応式

HRID 364920 の反応式
[Cl-].[NH4+].O.[CH3:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH2:16][CH:15]([C:17]3[CH:22]=[CH:21][C:20]([N+:23]([O-])=O)=[CH:19][CH:18]=3)[N:14]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[N:13]=2)=[CH:8][CH:7]=1>[Fe].C(O)(=O)C>[NH2:23][C:20]1[CH:21]=[CH:22][C:17]([CH:15]2[N:14]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[N:13]=[C:12]([C:9]3[CH:8]=[CH:7][C:6]([O:5][CH3:4])=[CH:11][CH:10]=3)[CH2:16]2)=[CH:18][CH:19]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 962WaterHCID 25517Ammonium ChlorideHCID 44365033-(4-Methoxyphenyl)-5-(4-nitrophenyl)-1-phenyl-2-pyrazoline

生成物 1

HCID 20155091HCID 20155091、化合物収率 80.5%

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 176Acetic Acid溶媒

実験手順

15.8 g of metallic iron powder and 1.6 g of ammonium chloride were dispersed in a mixed solution of 140 ml of iospropyl alcohol and 14 ml of water, and, while stirring and refluxing under heating, 13.1 g of 3-(4-methoxyphenyl)-5-(4-nitrophenyl)-1-phenyl-2-pyrazoline was added thereto. After refluxing for 2 hours, 10 ml of acetic acid was added thereto, and the reaction was thereafter continued for 30 minutes under refluxing. Solids were removed by filtration using sellaite, and 150 ml of water was added to the filtrate. Crystals precipitated were collected by filtration to obtain 9.7 g of 5-(4-aminophenyl)-3-(4-methoxyphenyl)-1-phenyl-2-pyrazoline. m.p. 164°-166° C.

後処理

  1. temperaturerefluxing
  2. temperatureunder heating
  3. temperatureAfter refluxing for 2 hours
  4. temperatureunder refluxing
  5. customSolids were removed by filtration
  6. additionwas added to the filtrate
  7. customCrystals precipitated
  8. filtrationwere collected by filtration

出典と根拠

ORDレコード
ord-d909a80332484beeb01e4d9f205cd1fd
出典データセット
uspto-grants-1986_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04607006

反応ノート

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