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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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Dimethylformamide diethylacetal → HCID 178484332、化合物

HRID 1931548
ノート
印刷プレビュー

反応式

HRID 1931548 の反応式
[C:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([NH2:9])=[O:8])=[CH:5][CH:4]=1)#[N:2].C(O[CH:15](OCC)[N:16]([CH3:18])[CH3:17])C>>[C:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7](/[N:9]=[CH:15]/[N:16]([CH3:18])[CH3:17])=[O:8])=[CH:5][CH:4]=1)#[N:2]
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

3

反応物 2

HCID 70913Dimethylformamide diethylacetalHCID 76427p-Cyanobenzamide

生成物 1

HCID 178484332HCID 178484332、化合物収率 96.1%

反応条件

温度
120 °C

実験手順

4-cyanobenzamide (327.0 mg, 2.237 mmol) and N,N-dimethylformamide diethyl acetal (0.53 ml, 3.09 mmol) were combined and heated to 120° C. A short path distillation apparatus was used to collect the ethanol that was liberated during the reaction. The reaction mixture was a dark purple solution that slowly turned lighter until it had become an amber solution. After 70 minutes, the reaction mixture solidified. The reaction mixture was cooled to room temperature and was placed under high vacuum overnight to give the title compound (432.7 mg, 2.150 mmol) as a yellow solid.

後処理

  1. distillation
A short path distillation apparatus
  • customto collect the ethanol that
  • customwas liberated during the reaction
  • temperatureThe reaction mixture was cooled to room temperature
  • customwas placed under high vacuum overnight
  • 出典と根拠

    ORDレコード
    ord-0f92734a7d6a4c9690d62b9518dabb0d
    出典データセット
    uspto-grants-2012_05
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08188085B2

    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