Hydrochloric Acid → Ethyl 3-oxo-3-(4-phenoxyphenyl)propanoate

HRID 1610454노트

반응식

HRID 1610454 반응식
[O:1]([C:8]1[CH:9]=[C:10]([CH:14]=[CH:15][CH:16]=1)C(O)=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N1C=CN=C1)(N1C=CN=C1)=O.[Mg+].[C:30]([O:36][CH2:37][CH3:38])(=[O:35])[CH2:31][C:32]([O-])=[O:33].Cl>O1CCCC1.O.C(OCC)(=O)C>[O:33]=[C:32]([C:14]1[CH:15]=[CH:16][C:8]([O:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)=[CH:9][CH:10]=1)[CH2:31][C:30]([O:36][CH2:37][CH3:38])=[O:35]

참가 물질

8

실험 절차

To a solution of 3-phenoxybenzoic acid (13.5 g, 63.0 mmol) in tetrahydrofuran (150 ml) was added 1,1′-carbonylbis-1H-imidazole (11.2 g, 69.3 mmol), and the mixture was stirred at room temperature for 30 min. To the reaction solution was added monoethyl malonate magnesium salt (10 g, 34.8 mmol) and the mixture was stirred at room temperature for 2 hrs. To the reaction solution were added ethyl acetate (50 ml) and water (50 ml), and conc. hydrochloric acid was added until the pH of the aqueous layer became acidic. The reaction solution was extracted with ethyl acetate (200 ml×2). The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to give ethyl 3-oxo-3-(4-phenoxyphenyl)propionate (17.9 g, 100%) as a brown oil.

후처리

  1. stirringthe mixture was stirred at room temperature for 2 hrs
  2. additionwas added until the pH of the aqueous layer
  3. extractionThe reaction solution was extracted with ethyl acetate (200 ml×2)
  4. washThe extract was washed with saturated brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customevaporated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1)

출처 및 근거

ORD 기록
ord-c1aea9e0fce54cde85ead9f0ebb1c733
출처 데이터셋
uspto-grants-2006_01
특허 번호
US06982348B2

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