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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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Diethyl Carbonate → Ethyl cyano(3,4-dimethoxyphenyl)acetate

HRID 1654162
ノート
印刷プレビュー

反応式

HRID 1654162 の反応式
[Na].[C:2](#[N:14])[CH2:3][C:4]1[CH:13]=[CH:12][C:9]([O:10][CH3:11])=[C:6]([O:7][CH3:8])[CH:5]=1.[C:15](=O)([O:19]CC)[O:16][CH2:17][CH3:18]>>[CH3:8][O:7][C:6]1[CH:5]=[C:4]([CH:3]([C:2]#[N:14])[C:15]([O:16][CH2:17][CH3:18])=[O:19])[CH:13]=[CH:12][C:9]=1[O:10][CH3:11]
参加物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 7766Diethyl CarbonateHCID 667273,4-DimethoxybenzeneacetonitrileHCID 5360545Sodium

生成物 1

HCID 12814070Ethyl cyano(3,4-dimethoxyphenyl)acetate

実験手順

25.7 g (1.1 mol eq.) of sodium in small pieces were added gradually to a solution of 198 g (1.1 mol) of homoveratronitrile in 500 ml of diethyl carbonate in such a manner that the temperature remained at approximately 100°. Thereafter, the reaction mixture was heated to reflux for 1 hour, evaporated under reduced pressure, treated with cooled water, acidified with 70 ml of glacial acetic acid and extracted with ether. The combined organic extracts were dried and evaporated. The residual oil Was distilled in a high vacuum, whereby ethyl 3,4-dimethoxyphenylcyanoacetate was obtained, b.p. 170°-172°/70 Pa. HPLC purity >99%.

後処理

  1. customremained at approximately 100°
  2. temperatureThereafter, the reaction mixture was heated
  3. temperatureto reflux for 1 hour
  4. customevaporated under reduced pressure
  5. additiontreated with cooled water
  6. extractionextracted with ether
  7. customThe combined organic extracts were dried
  8. customevaporated
  9. distillationThe residual oil Was distilled in a high vacuum

出典と根拠

ORDレコード
ord-5bd4e871ed42498eac4fa4b9bd884ae8
出典データセット
uspto-grants-1995_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05405866

反応ノート

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