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Methyl 3,5-diethoxy-4-methoxybenzoate → HCID 68698382, 화합물

HRID 1990885
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HRID 1990885 반응식
C[O:2][C:3](=O)[C:4]1[CH:9]=[C:8]([O:10][CH2:11][CH3:12])[C:7]([O:13][CH3:14])=[C:6]([O:15][CH2:16][CH3:17])[CH:5]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[CH2:16]([O:15][C:6]1[CH:5]=[C:4]([CH2:3][OH:2])[CH:9]=[C:8]([O:10][CH2:11][CH3:12])[C:7]=1[O:13][CH3:14])[CH3:17]
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참가 물질

4

반응물 2

HCID 20095711Methyl 3,5-diethoxy-4-methoxybenzoateHCID 21226445Aluminium lithium hydride

생성물 1

HCID 68698382HCID 68698382, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 3,5-diethoxy-4-methoxy-benzoic acid methyl ester (0.34 g, 1.34 mmol, 1.0 equiv; prepared as described in EP 0 419 905 B1, Eisai Co.) in anhydrous THF (5 mL) was added lithium aluminium hydride (0.15 g, 4.01 mmol, 3.0 equiv) and the reaction mixture stirred at rt for 4 h. The crude reaction mixture was filtered over Hyflo Super Cel, the filtrate extracted with diethyl ether (3×50 mL) and the combined organic phases dried over MgSO4 providing 0.26 g (86%) of the title compound. 1H NMR (300 MHz, CDCl3): δ 1.36 (t, J=7.0 Hz, 6H), 3.77 (s, 3H), 4.02 (q, J=7.0 Hz, 4H), 4.53 (s, 2H), 6.51 (s, 2H). MS (EI): 227.3 [M]+.

후처리

  1. customThe crude reaction mixture
  2. filtrationwas filtered over Hyflo Super Cel
  3. extractionthe filtrate extracted with diethyl ether (3×50 mL)
  4. dry with materialthe combined organic phases dried over MgSO4 providing 0.26 g (86%) of the title compound

출처 및 근거

ORD 기록
ord-9b4e5dcd64ec4d6fb026e83c8fbe29c0
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07645753B2

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