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Water → 6-But-2-ynyloxy-benzofuran-2-carboxlic acid ethyl ester

HRID 1171205
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HRID 1171205 반응식
[CH2:1]([O:3][C:4]([C:6]1[O:7][C:8]2[CH:14]=[C:13]([OH:15])[CH:12]=[CH:11][C:9]=2[CH:10]=1)=[O:5])[CH3:2].[H-].[Na+].Br[CH2:19][C:20]#[C:21][CH3:22].O>O1CCCC1.CN(C)C=O>[CH2:1]([O:3][C:4]([C:6]1[O:7][C:8]2[CH:14]=[C:13]([O:15][CH2:19][C:20]#[C:21][CH3:22])[CH:12]=[CH:11][C:9]=2[CH:10]=1)=[O:5])[CH3:2]
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참가 물질

7

반응물 4

HCID 962WaterHCID 24758Sodium hydrideHCID 27568621-Bromo-2-butyneHCID 66786469Ethyl 6-hydroxybenzofuran-2-carboxylate

생성물 1

HCID 576082296-But-2-ynyloxy-benzofuran-2-carboxlic acid ethyl ester수율 81%

시약·촉매·용매 2

HCID 6228Dimethylformamide
용매
HCID 8028Tetrahydrofuran용매

실험 절차

To a mixed solution of 6-hydroxy-benzofuran-2-carboxylic acid ethyl ester (250 mg, 1.21 mmol) in tetrahydrofuran (5 mL) and N,N-dimethylformamide (5 mL) were added sodium hydride (58 mg, 2.42 mmol) and 1-bromo-2-butyne (127 μL) at room temperature, which was stirred at room temperature for 1 hour. Water was added to the reaction solution followed by extraction with ethyl acetate. The organic layer was washed with water and sat. NaCl followed by drying over anhydrous magnesium sulfate and filtering. The filtrate was concentrated under a reduced pressure and the residue was purified by silica gel column chromatography (heptane:ethyl acetate=5:1) to obtain the title compound (254 mg, 81%) as a white solid.

후처리

  1. extractionfollowed by extraction with ethyl acetate
  2. washThe organic layer was washed with water and sat. NaCl
  3. dry with materialby drying over anhydrous magnesium sulfate
  4. filtrationfiltering
  5. concentrationThe filtrate was concentrated under a reduced pressure
  6. customthe residue was purified by silica gel column chromatography (heptane:ethyl acetate=5:1)

출처 및 근거

ORD 기록
ord-3745deb4c8f3495080f95eab01c48d8b
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07829585B2

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