Iodoethane → 4-Ethoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester

HRID 29344노트

반응식

HRID 29344 반응식
[CH2:1]([O:3][C:4]([C:6]1[O:7][C:8]2[CH:15]=[CH:14][CH:13]=[C:12]([OH:16])[C:9]=2[C:10]=1[CH3:11])=[O:5])[CH3:2].[CH2:17](I)[CH3:18].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[CH2:1]([O:3][C:4]([C:6]1[O:7][C:8]2[CH:15]=[CH:14][CH:13]=[C:12]([O:16][CH2:17][CH3:18])[C:9]=2[C:10]=1[CH3:11])=[O:5])[CH3:2]

참가 물질

5

반응물 3

HCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 748649Ethyl 4-hydroxy-3-methyl-1-benzofuran-2-carboxylate

생성물 1

HCID 687122294-Ethoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester수율 77%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

4-Hydroxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester (200 mg) was mixed with ethyl iodide (0.5 mL), K2CO3 (200 mg) and 2 mL of DMF. The mixture was stirred at room temperature overnight. The mixture was washed with brine and extracted with ethyl acetate. The combined ethyl acetate layers were washed with brine. Removal of the solvent under vacuum gave the crude product, which was purified by column chromatography to give 175 mg (77% yield) of 4-ethoxy-3-methyl-benzofuran-2-carboxylic acid ethyl ester as white solid.

후처리

  1. washThe mixture was washed with brine
  2. extractionextracted with ethyl acetate
  3. washThe combined ethyl acetate layers were washed with brine
  4. customRemoval of the solvent under vacuum
  5. customgave the crude product, which
  6. customwas purified by column chromatography

출처 및 근거

ORD 기록
ord-51573b178c954b40b9c923f866c5ba9f
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07420001B2

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