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Ethyl Acetate → 3-Methoxybutyl 2,3,4,5,6-pentafluorobenzenesulfonate

HRID 1886762
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HRID 1886762 반응식
[CH3:1][O:2][CH:3]([CH3:7])[CH2:4][CH2:5][OH:6].[F:8][C:9]1[C:14]([S:15](Cl)(=[O:17])=[O:16])=[C:13]([F:19])[C:12]([F:20])=[C:11]([F:21])[C:10]=1[F:22].C([O-])(O)=O.[Na+].C(OCC)(=O)C>C(Cl)Cl>[F:8][C:9]1[C:10]([F:22])=[C:11]([F:21])[C:12]([F:20])=[C:13]([F:19])[C:14]=1[S:15]([O:6][CH2:5][CH2:4][CH:3]([O:2][CH3:1])[CH3:7])(=[O:17])=[O:16]
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참가 물질

6

반응물 4

HCID 8857Ethyl AcetateHCID 172913-Methoxy-1-butanolHCID 700262,3,4,5,6-Pentafluorobenzenesulfonyl chlorideHCID 516892Sodium Bicarbonate

생성물 1

HCID 867619853-Methoxybutyl 2,3,4,5,6-pentafluorobenzenesulfonate수율 38.9%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

To a solution of 3-methoxybutane-1-ol (0.78 g, 7.5 mmol) and TEA (0.388 g, 3.8 mmol), in CH2Cl2 (15 mL) was added pentafluorobenzenesulfonyl chloride (0.79 g, 3.0 mmol). The solution was stirred at rt for 4 h. Saturated aqueous NaHCO3 (10 mL) was added to the solution and the mixture was stirred at rt for 30 min. The organics were extracted with CH2Cl2 (30 mL) and washed with 0.5 M HCl (2×20 mL) and saturated aqueous NaCl (1×20 mL). The organics were dried over Na2SO4 and concentrated to give a crude mixture. Silica gel chromatography (15% ethyl acetate in hexanes) yielded the desired product (0.39 g, 36%). 1H NMR (400 MHz CDCl3) δ 4.40 (m, 2H), 3.45 (m, 1H), 3.26 (s, 3H), 1.87 (m, 2H), 1.15 (d, 3H, J=6.1 Hz). Anal. Calcd. For C11H11F5O4S: C, 39.53; H, 3.32. Found: C, 39.83; H, 3.45.

후처리

  1. stirringthe mixture was stirred at rt for 30 min
  2. extractionThe organics were extracted with CH2Cl2 (30 mL)
  3. washwashed with 0.5 M HCl (2×20 mL) and saturated aqueous NaCl (1×20 mL)
  4. dry with materialThe organics were dried over Na2SO4
  5. concentrationconcentrated
  6. customto give a crude mixture

출처 및 근거

ORD 기록
ord-311afde7e0c54d5ca70e99ef09ee9b3a
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501382B1

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