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Potassium Carbonate → Ethyl 5-methyl-1-benzofuran-2-carboxylate

HRID 1773225
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HRID 1773225 반응식
[CH:1]([C:3]1[CH:15]=[C:14]([CH3:16])[CH:13]=[CH:12][C:4]=1[O:5][CH2:6][C:7]([O:9][CH2:10][CH3:11])=[O:8])=O.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[CH3:16][C:14]1[CH:13]=[CH:12][C:4]2[O:5][C:6]([C:7]([O:9][CH2:10][CH3:11])=[O:8])=[CH:1][C:3]=2[CH:15]=1
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참가 물질

4

반응물 2

HCID 11430Potassium CarbonateHCID 13157005Ethyl (2-formyl-4-methylphenoxy)acetate

생성물 1

HCID 13157013Ethyl 5-methyl-1-benzofuran-2-carboxylate수율 58.3%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
90 °C

실험 절차

To a solution of ethyl 2-(2-formyl-4-methylphenoxy)acetate (2.24 g, 10.08 mmol) in 15 mL of DMF was added K2CO3 (2.79 g, 20.16 mmol), the mixture was stirred under nitrogen at 90° C. for 3 hr. After cooling to room temperature, the mixture was filtered through Celite, and washed with DCM. The combined filtrate was concentrated, and the resulting residue was purified by silica gel flash chromatography, 100% Heptane-20% Ethyl Acetate/80% Heptane, to give a white solid, ethyl 5-methylbenzofuran-2-carboxylate (1.2 g). LCMS retention time=1.54 minutes (LC method 3); MS (m+1)=204.8. 1H NMR (400 MHz, DMSO-d6) δ 1.33 (t, J=7.1 Hz, 3H), 2.41 (s, 3H), 4.35 (q, J=7.1 Hz, 2H), 7.34 (dd, J=8.5, 1.4 Hz, 1H), 7.55-7.63 (m, 2H), 7.68 (d, J=0.9 Hz, 1H).

후처리

  1. temperatureAfter cooling to room temperature
  2. filtrationthe mixture was filtered through Celite
  3. washwashed with DCM
  4. concentrationThe combined filtrate was concentrated
  5. customthe resulting residue was purified by silica gel flash chromatography, 100% Heptane-20% Ethyl Acetate/80% Heptane

출처 및 근거

ORD 기록
ord-dcb5d7eb4ac9455d94d36ce52a92f51a
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09255093B2

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