4-Bromo-2-methylbut-1-ene → 2-Methoxy-1-[2,4,6-trihydroxy-3,5-di(3-methyl-2-buten-1-yl)phenyl]ethanone

HRID 1528034

반응식

HRID 1528034 반응식
[CH3:1][O:2][CH2:3][C:4]([C:6]1[C:11]([OH:12])=[CH:10][C:9]([OH:13])=[CH:8][C:7]=1[OH:14])=[O:5].[CH2:15](Br)[CH2:16][C:17]([CH3:19])=[CH2:18]>[OH-].[K+]>[CH3:1][O:2][CH2:3][C:4]([C:6]1[C:7]([OH:14])=[C:8]([CH2:15][CH:16]=[C:17]([CH3:19])[CH3:18])[C:9]([OH:13])=[C:10]([CH2:3][CH:4]=[C:6]([CH3:11])[CH3:7])[C:11]=1[OH:12])=[O:5]

참가 물질

4

반응물 2

HCID 5495854-Bromo-2-methylbut-1-eneHCID 6434002-Methoxy-1-(2,4,6-trihydroxyphenyl)ethanone

생성물 1

HCID 867022152-Methoxy-1-[2,4,6-trihydroxy-3,5-di(3-methyl-2-buten-1-yl)phenyl]ethanone수율 41%

시약·촉매·용매 1

HCID 14797Potassium Hydroxide용매

실험 절차

2-methoxy-1-(2,4,6-trihydroxyphenyl)ethanone (8.3 g, 42 mmol) was dissolved in a 5% potassium hydroxide aqueous solution (84 ml). After the reaction mixture was cooled below 0° C., Isopentenyl bromide (12.48 g, 84 mmol) was slowly added dropwise to within 30 minutes. The reaction mixture was stirred at room temperature (RT) for 2 hours, then poured into an ice water and acidified to pH 2. The reaction mixture was extracted with ethyl acetate. The extract was collected and dried over anhydrous sodium sulfate, followed by removing solvent. The desired compound was obtained by purifying the residue by silica gel column chromatography (dichloromethane as eluent) (5.7 g, yield 41%). 1H NMR (400 MHz, DMSO-d6): δ=11.44 (s, 2H), 9.24 (s, 1H), 5.00 (t, 2H, J=6.8 Hz), 4.63 (s, 2H,), 3.31 (s, 3H), 3.22 (d, 4H, J=6.8 Hz), 1.67 (s, 6H), 1.58 (s, 6H).

후처리

  1. temperatureAfter the reaction mixture was cooled below 0° C.
  2. extractionThe reaction mixture was extracted with ethyl acetate
  3. customThe extract was collected
  4. dry with materialdried over anhydrous sodium sulfate
  5. customby removing solvent

출처 및 근거

ORD 기록
ord-53f269416ed1433b81d3fd78cfd8b932
출처 데이터셋
uspto-grants-2015_07
특허 번호
US09090583B2

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