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Ethanol → Ethyl 4-trichloroacetamido-5-hexenoate

HRID 1756318
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HRID 1756318 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

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

생성물 1

HCID 11055787Ethyl 4-trichloroacetamido-5-hexenoate수율 727.1%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-d30538f9dcbb48e9bf7c406f3f9d36d4
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05440065

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