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Ethanol → Ethyl 4-trichloroacetamido-5-hexenoate

HRID 1721740
ノート
印刷プレビュー

反応式

HRID 1721740 の反応式
[H-].[Na+].O[CH2:4][CH:5]=[CH:6][CH2:7][CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10].[Cl:14][C:15]([Cl:19])([Cl:18])[C:16]#[N:17].C([OH:22])C>CCOCC>[Cl:14][C:15]([Cl:19])([Cl:18])[C:16]([NH:17][CH:6]([CH:5]=[CH2:4])[CH2:7][CH2:8][C:9]([O:11][CH2:12][CH3:13])=[O:10])=[O:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 702EthanolHCID 11011TrichloroacetonitrileHCID 24758Sodium hydrideHCID 53641333Ethyl 6-hydroxy-4-hexenoate

生成物 1

HCID 11055787Ethyl 4-trichloroacetamido-5-hexenoate収率 727.1%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

Sodium hydride (0.03 g of a 50% dispersion in oil, 0.5 mmol, was added to a solution of ethyl 6-hydroxy-4-hexenoate (0.7 g, 5 mmol) and trichloroacetonitrile (0.6 g, 5 mmol) in anhydrous ether (50 mL) under N2 at 0° C. After 1 H, ethanol (0.5 mmol) was added and the solvent was removed in vacuo. The formation of the imidate was controled by NMR (NH,~8.5 ppm). A solution of the crude imidate in xylene (30 mL) was heated at reflux 48 H. Then the solvent was removed in vacuo and the residue was purified by flash chromatography on SiO2. (eluant AcOEt: hexane, 2:8) to give the title product (1.1 g, ~70%).

後処理

  1. customthe solvent was removed in vacuo
  2. temperatureA solution of the crude imidate in xylene (30 mL) was heated
  3. temperatureat reflux 48 H
  4. customThen the solvent was removed in vacuo
  5. customthe residue was purified by flash chromatography on SiO2

出典と根拠

ORDレコード
ord-d680ef5728934538954b638cdecc0195
出典データセット
uspto-grants-1996_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05512698

反応ノート

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