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Methanol → Methyl 5-methoxy-1-benzofuran-2-carboxylate

HRID 713739
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HRID 713739 반응식
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[O:10][C:9]([C:11]([OH:13])=[O:12])=[CH:8][C:7]=2[CH:14]=1.[CH3:15]O.S(Cl)(Cl)=O>O>[CH3:15][O:12][C:11]([C:9]1[O:10][C:6]2[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:14][C:7]=2[CH:8]=1)=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 2886385-Methoxybenzofuran-2-carboxylic acid

생성물 1

HCID 14916651Methyl 5-methoxy-1-benzofuran-2-carboxylate

시약·촉매·용매 1

HCID 962Water용매

실험 절차

5-Methoxybenzofuran-2-carboxylic acid (5.04 g, 26 mmol) was weighed into a 200 ml round bottom flask fitted with a stir bar, septum and nitrogen inlet. Anhydrous MeOH (50 ml) was added under nitrogen atmosphere. The solution was cooled in an ice bath and thionyl chloride (2.3 ml, 32 mmol) was added dropwise with vigorous stirring. After stirring for 72 h at room temperature, the reaction mixture was poured into water (150 ml) and the white solid was collected. The solid was dissolved in toluene (100 ml) and the solution was washed with 1M NaHCO3 and brine and dried over MgSO4. Removal of the organic layer provided 5-methoxybenzofuran-2-carboxylic acid methyl ester as a white solid (5.15 g).

후처리

  1. customfitted with a stir bar
  2. temperatureThe solution was cooled in an ice bath
  3. customthe white solid was collected
  4. dissolutionThe solid was dissolved in toluene (100 ml)
  5. washthe solution was washed with 1M NaHCO3 and brine
  6. dry with materialdried over MgSO4
  7. customRemoval of the organic layer

출처 및 근거

ORD 기록
ord-df9b12305cee4ea9b98e117ef25469f9
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09186347B1

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