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Hydrochloric Acid → (E)-3-ethoxy-N-(3-methoxy-4-nitro-phenyl)-acrylamide

HRID 1773560
ノート
印刷プレビュー

反応式

HRID 1773560 の反応式
S(Cl)(Cl)=O.C(O[CH:8]([O:13][CH2:14][CH3:15])[CH2:9][C:10]([OH:12])=O)C.[CH3:16][O:17][C:18]1[CH:19]=[C:20]([NH2:27])[CH:21]=[CH:22][C:23]=1[N+:24]([O-:26])=[O:25].N1C=CC=CC=1.Cl>ClCCl>[CH2:14]([O:13]/[CH:8]=[CH:9]/[C:10]([NH:27][C:20]1[CH:21]=[CH:22][C:23]([N+:24]([O-:26])=[O:25])=[C:18]([O:17][CH3:16])[CH:19]=1)=[O:12])[CH3:15]
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

7

反応物 5

HCID 313Hydrochloric AcidHCID 1049PyridineHCID 24386Thionyl ChlorideHCID 4152823,3-Diethoxypropanoic acidHCID 27557953-Methoxy-4-nitroaniline

生成物 1

HCID 66664739(E)-3-ethoxy-N-(3-methoxy-4-nitro-phenyl)-acrylamide収率 109.7%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
80 °C

実験手順

Thionyl chloride (1 mL) was added to 3,3-diethoxy-propionic acid (Eur. J. Org. Chem. 2001, 2041) (0.20 g, 1.10 mmol) and the resulting mixture was heated at 80° C. for 1 hour. The reaction mixture was then evaporated under reduced pressure and the residue was dissolved in dichloromethane (2 mL). The resulting solution was added to a mixture of 3-methoxy-4-nitro-phenylamine (0.13 g, 0.77 mmol) and pyridine (0.12 g, 1.54 mmol) in dichloromethane (5 mL) at 0° C. The reaction mixture was stirred at room temperature overnight and then the pH was then neutralized by addition of an aqueous solution of hydrochloric acid (6 M). The resulting mixture was extracted twice with ethyl acetate and the combined organic extracts were washed with water, dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to give 225 mg of (E)-3-ethoxy-N-(3-methoxy-4-nitro-phenyl)-acrylamide as an orange solid.

後処理

  1. customThe reaction mixture was then evaporated under reduced pressure
  2. dissolutionthe residue was dissolved in dichloromethane (2 mL)
  3. extractionThe resulting mixture was extracted twice with ethyl acetate
  4. washthe combined organic extracts were washed with water
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-e3f470c97fd94970b770cfd08de36cbf
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09255110B2

反応ノート

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