Hydrochloric Acid → Ethyl 4-methoxy-3-methyl-2-benzofurancarboxylate

HRID 1084853ノート

反応式

HRID 1084853 の反応式
[CH3:1][C:2]1[C:6]2[C:7]([OH:11])=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][C:3]=1[C:12]([O:14][CH2:15][CH3:16])=[O:13].[C:17]([O-])([O-])=O.[K+].[K+].CI.Cl>CC(C)=O.O>[CH3:1][C:2]1[C:6]2[C:7]([O:11][CH3:17])=[CH:8][CH:9]=[CH:10][C:5]=2[O:4][C:3]=1[C:12]([O:14][CH2:15][CH3:16])=[O:13]

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 748649Ethyl 4-hydroxy-3-methyl-1-benzofuran-2-carboxylate

生成物 1

HCID 9497663Ethyl 4-methoxy-3-methyl-2-benzofurancarboxylate

試薬・触媒・溶媒 2

HCID 180Acetone溶媒HCID 962Water溶媒

実験手順

To a solution of ethyl 3-methyl-4-hydroxybenzofuran-2-carboxylate 20 (5.02 g, 22.8 mmol) in acetone (85 mL) was added sequentially K2CO3 (6.3 g, 45.6 mmol) and methyl iodide (6.47 g, 45.6 mmol). The resulting suspension was heated to reflux with stirring for 15 hours, allowed to cool, diluted with water (125 mL), and acidified with 2N HCl (50 mL). The resulting mixture was extracted with ethyl acetate (1×100 mL then 2×50 mL) and the combined extracts were dried and concentrated to a brown oil. Chromatographic purification (Preparative HPLC, 5% ethyl acetate in hexane as eluant) afforded pure ethyl 3-methyl-4-methoxybenzofuran-2-carboxylate as a colorless oil which crystallized on standing. mp 67°-69° C.; 1H NMR d 1.47 (3H, t, J=6 Hz), 2.78 (3H, s), 3.96 (3H, s), 4.48 (2H, q, J=6 Hz), 6.66 (1H, d, J=8 Hz), 7.16 (1H, d, J=8 Hz), 7.36 (1H, t, J=8 Hz).

後処理

  1. temperatureThe resulting suspension was heated
  2. temperatureto reflux
  3. temperatureto cool
  4. extractionThe resulting mixture was extracted with ethyl acetate (1×100 mL
  5. custom2×50 mL) and the combined extracts were dried
  6. concentrationconcentrated to a brown oil
  7. customChromatographic purification (Preparative HPLC, 5% ethyl acetate in hexane as eluant)

出典と根拠

ORDレコード
ord-e83c16cf1ca94e40a4f6a96a73a81679
出典データセット
uspto-grants-1991_04
特許番号
US05006549

反応ノート

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