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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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Ethanol → HCID 70817737、化合物

HRID 1753097
ノート
印刷プレビュー

反応式

HRID 1753097 の反応式
[OH-:1].[Na+].[CH:3]([N:6]1[C:10]([C:11]([F:14])([F:13])[F:12])=[C:9](CC#N)[CH:8]=[N:7]1)([CH3:5])[CH3:4].[CH3:18][CH2:19][OH:20]>>[CH:3]([N:6]1[C:10]([C:11]([F:14])([F:13])[F:12])=[C:9]([CH2:18][C:19]([OH:1])=[O:20])[CH:8]=[N:7]1)([CH3:5])[CH3:4]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 70817665HCID 70817665、化合物

生成物 1

HCID 70817737HCID 70817737、化合物収率 75%

反応条件

温度
60 °C

実験手順

Aqueous sodium hydroxide (150 mL of a 1 M solution) was added to [1-isopropyl-5-(trifluoromethyl)-1H-pyrazol-4-yl]acetonitrile (Preparation 106, 6.2 g, 28.6 mmol) in EtOH (150 mL) and the mixture was heated at 60° C. for 16 hours. The mixture was evaporated in vacuo and the residue was dissolved in water (50 mL) then washed with EtOAc (100 mL). The aqueous phase was acidified to pH 5 using 1N HCl and extracted with 10% IPA in DCM (4×100 mL). The combined organic phases were dried over sodium sulphate and evaporated in vacuo to afford the title compound as a white solid in 75% yield, 5.0 g.

後処理

  1. customThe mixture was evaporated in vacuo
  2. dissolutionthe residue was dissolved in water (50 mL)
  3. washthen washed with EtOAc (100 mL)
  4. extractionextracted with 10% IPA in DCM (4×100 mL)
  5. dry with materialThe combined organic phases were dried over sodium sulphate
  6. customevaporated in vacuo

出典と根拠

ORDレコード
ord-5b8b9bc7730c4e9fb8c47860be77d4c6
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09163021B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート