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

HRID 1773225
ノート
印刷プレビュー

反応式

HRID 1773225 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

HCID 13157013Ethyl 5-methyl-1-benzofuran-2-carboxylate収率 58.3%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
90 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-dcb5d7eb4ac9455d94d36ce52a92f51a
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09255093B2

反応ノート

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