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Ethanol → HCID 13882127、化合物

HRID 867375
ノート
印刷プレビュー

反応式

HRID 867375 の反応式
[C:1]([C:3]1[N:7]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([F:14])[CH:9]=2)[N:6]=[CH:5][C:4]=1[C:15]([O:17]CC)=[O:16])#[N:2].[OH-].[K+].C([OH:24])C>O>[C:15]([C:4]1[CH:5]=[N:6][N:7]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([F:14])[CH:9]=2)[C:3]=1[C:1]([NH2:2])=[O:24])([OH:17])=[O:16]
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 702EthanolHCID 14797Potassium HydroxideHCID 13772971ethyl 5-cyano-1-(3-fluorophenyl)-1H-pyrazole-4-carboxylate

生成物 1

HCID 13882127HCID 13882127、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A 5.5 g. portion of ethyl 5-cyano-1-(3-fluorophenyl)-4-pyrazolecarboxylate and 4.7 g. of potassium hydroxide were dissolved in 100 ml. of ethanol at the reflux temperature and the mixture was stirred at that temperature for2 hours. The mixture was then diluted to 350 ml. with cold water, and was heated slightly to obtain a solution which was made acid with concentratedhydrochloric acid. The product was precipitated by adding small amounts of ice, and the precipitated product was then collected by filtration and crystallized from ethanol-water to obtain 3.6 g. of the desired product, m.p. 215°-216°, having the following elemental analysis.

後処理

  1. additionThe mixture was then diluted to 350 ml
  2. customto obtain a solution which
  3. customThe product was precipitated
  4. additionby adding small amounts of ice
  5. filtrationthe precipitated product was then collected by filtration
  6. customcrystallized from ethanol-water
  7. customto obtain 3.6 g

出典と根拠

ORDレコード
ord-49179e162c62423e8ff31e70075bb35c
出典データセット
uspto-grants-1988_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04775409

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