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Toluene → 3-(4-Diethylamino-2-hydroxy-phenyl)-but-2-enoic acid ethyl ester

HRID 655067
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HRID 655067 반응식
[CH2:1]([O:3][C:4](C=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)=[O:5])[CH3:2].[CH2:26]([N:28]([CH2:39][CH3:40])[C:29]1[CH:34]=[CH:33][C:32]([C:35](=O)[CH3:36])=[C:31]([OH:38])[CH:30]=1)[CH3:27].[C:41]1(C)C=CC=CC=1>>[CH2:1]([O:3][C:4](=[O:5])[CH:36]=[C:35]([C:32]1[CH:33]=[CH:34][C:29]([N:28]([CH2:39][CH3:40])[CH2:26][CH3:27])=[CH:30][C:31]=1[OH:38])[CH3:41])[CH3:2]
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참가 물질

4

반응물 3

HCID 1140TolueneHCID 70670Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 47370991-(4-Diethylamino-2-hydroxy-phenyl)-ethanone

생성물 1

HCID 540390873-(4-Diethylamino-2-hydroxy-phenyl)-but-2-enoic acid ethyl ester

실험 절차

To a suspension of 5.27 g ethoxycarbonylmethylenetriphenylphosphorane in 10 ml of toluene, a solution of 2.02 g 1-(4-diethylamino-2-hydroxy-phenyl)ethanone (DE 28 44 606) was dropped in at room temperature. Then the reaction mixture was heated to reflux. After refluxing for 31 hours the mixture was cooled down and evaporated to dryness. The resulting dark oil was purified by chromatography to yield a colourless oil.

후처리

  1. temperatureThen the reaction mixture was heated to reflux
  2. temperatureAfter refluxing for 31 hours the mixture
  3. temperaturewas cooled down
  4. customevaporated to dryness
  5. customThe resulting dark oil was purified by chromatography
  6. customto yield a colourless oil

출처 및 근거

ORD 기록
ord-6341323ae66147b3b237f867cf3338d6
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE043006E1

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