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Ethanol → HCID 14944863, 화합물

HRID 1505762
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HRID 1505762 반응식
[Br:1][C:2]1[CH:3]=[C:4]([C:11]([OH:13])=[O:12])[C:5]2[O:9][CH2:8][CH2:7][C:6]=2[CH:10]=1.[CH3:14][CH2:15]O>S(=O)(=O)(O)O>[Br:1][C:2]1[CH:3]=[C:4]([C:11]([O:13][CH2:14][CH3:15])=[O:12])[C:5]2[O:9][CH2:8][CH2:7][C:6]=2[CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 702EthanolHCID 27947975-bromo-2,3-dihydrobenzofuran-7-carboxylic Acid

생성물 1

HCID 14944863HCID 14944863, 화합물

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

To a solution of 5-bromo-2,3-dihydro-1-benzofuran-7-carboxylic acid (1.0 g) in EtOH (15 mL), sulfuric acid (0.5 mL) was added, and the solution was heated at reflux for 30 hours. The reaction mixture was cooled to room temperature, and EtOH was removed. To the residue was added water, and the solution was extracted with ethyl acetate. The ethyl acetate layer was washed sequentially with saturated aqueous sodium bicarbonate and brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to obtain the titled compound (1.07 g) as pale yellow powder.

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후처리

  1. temperaturethe solution was heated
  2. temperatureat reflux for 30 hours
  3. customEtOH was removed
  4. additionTo the residue was added water
  5. extractionthe solution was extracted with ethyl acetate
  6. washThe ethyl acetate layer was washed sequentially with saturated aqueous sodium bicarbonate and brine
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customThe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-df5d4b1ac50d448987c4d82febe70205
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09216968B2

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