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Boron trifluoride etherate → 6-Methoxy-1-benzothiophene

HRID 252158
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HRID 252158 반응식
B(F)(F)F.CCOCC.[CH3:10][O:11][C:12]1[CH:13]=[C:14]([S:18][CH2:19][CH:20]=O)[CH:15]=[CH:16][CH:17]=1.C(=O)(O)[O-].[Na+]>ClCCl>[CH3:10][O:11][C:12]1[CH:17]=[CH:16][C:15]2[CH:20]=[CH:19][S:18][C:14]=2[CH:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8000Boron trifluoride etherateHCID 516892Sodium BicarbonateHCID 13642522(3-Methoxyphenylsulphanyl)acetaldehyde

생성물 1

HCID 136342376-Methoxy-1-benzothiophene수율 61%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

반응 조건

온도
0 °C

실험 절차

Boron trifluoride etherate (8.15 mL) dissolved in dry dichloromethane (407 mL) was stirred rapidly at 0° C. under nitrogen and a solution of (3-methoxyphenylsulphanyl)acetaldehyde (11.5 g, 63.10 mmol) in dry dichloromethane (29 mL) was added dropwise over 25 min. The resultant green solution was stirred for 2 min and then saturated aqueous sodium bicarbonate solution (150 mL) was added at a rate so as to maintain the temperature <8° C. The reaction mixture was stirred for 5 min and then the layers were separated and the organic layer was washed with saturated aqueous sodium bicarbonate solution (100 mL) and water (100 mL). The organic phase was dried (MgSO4), and concentrated in vacuo. The product was purified by distillation to afford the title compound as a colourless oil (6.29 g, 61%, b.p. 83-88° C. at 16 mBar).

후처리

  1. stirringThe resultant green solution was stirred for 2 min
  2. temperatureto maintain the temperature <8° C
  3. stirringThe reaction mixture was stirred for 5 min
  4. customthe layers were separated
  5. washthe organic layer was washed with saturated aqueous sodium bicarbonate solution (100 mL) and water (100 mL)
  6. dry with materialThe organic phase was dried (MgSO4)
  7. concentrationconcentrated in vacuo
  8. distillationThe product was purified by distillation

출처 및 근거

ORD 기록
ord-b895cfdf07434aa0b96cdc991f555e2b
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07868017B2

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