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Methyl 1-benzofuran-5-carboxylate → 1-Benzofuran-5-Carboxylic Acid

HRID 2181646
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HRID 2181646 반응식
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]([O:12]C)=[O:11])=[CH:9][C:4]=2[CH:3]=[CH:2]1>CO.[OH-].[Na+]>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]([OH:12])=[O:11])=[CH:9][C:4]=2[CH:3]=[CH:2]1
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참가 물질

4

반응물 1

HCID 12674941Methyl 1-benzofuran-5-carboxylate

생성물 1

HCID 5956561-Benzofuran-5-Carboxylic Acid수율 100.3%

시약·촉매·용매 2

HCID 887Methanol용매HCID 14798Sodium Hydroxide용매

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온도
65 °C

실험 절차

A stirred mixture of methyl benzofuran-5-carboxylate (1.3 g, 7.38 mmol) in MeOH (51 mL) and sodium hydroxide (41 mL of a 5% aqueous solution) is heated to 65° C. for 4 h. The mixture is cooled to rt, and MeOH is removed in vacuo. The remaining aqueous layer is extracted with CH2Cl2. The CH2Cl2 layer is discarded, and the aqueous layer is acidified to pH=1 with concentrated hydrochloric acid. The aqueous layer is extracted with CHCl3. The organic layer is washed with water, dried (MgSO4), filtered and concentrated in vacuo to afford 1.2 g (98%) of benzofuran-5-carboxylic acid as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 12.9, 8.30, 8.11, 7.92, 7.69, 7.09.

후처리

  1. temperatureThe mixture is cooled to rt
  2. customMeOH is removed in vacuo
  3. extractionThe remaining aqueous layer is extracted with CH2Cl2
  4. extractionThe aqueous layer is extracted with CHCl3
  5. washThe organic layer is washed with water
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-f3d97d2bfe95416cb6771756392a4b84
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06894042B2

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