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4-Nitrophenethyl alcohol → 1-(2-Fluoroethyl)-4-nitrobenzene

HRID 1371269
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HRID 1371269 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][CH2:11]O)=[CH:6][CH:5]=1)([O-:3])=[O:2].C(N(S(F)(F)[F:19])CC)C.C(=O)([O-])O.[Na+]>C(Cl)Cl>[F:19][CH2:11][CH2:10][C:7]1[CH:8]=[CH:9][C:4]([N+:1]([O-:3])=[O:2])=[CH:5][CH:6]=1
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참가 물질

5

반응물 3

HCID 74944-Nitrophenethyl alcoholHCID 123472(Diethylamino)sulfur trifluorideHCID 516892Sodium Bicarbonate

생성물 1

HCID 148090071-(2-Fluoroethyl)-4-nitrobenzene

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of 2-(4-nitrophenyl)ethanol (835 mg) in methylene chloride (30 mL) was stirred at −78° C. under a nitrogen atomosphere. To this solution, diethylaminosulfur trifluoride (1.98 mL) in methylene chloride (20 mL) was added dropwise over 10 minutes. With stirring, the temperature of the reaction mixture was allowed to rise back to room temperature. After 30 minutes, the reaction was stopped by the addition of saturated aqueous sodium hydrogen carbonate solution (50 mL) in an ice bath. The methylene chloride solution was washed with saturated aqueous sodium hydrogen carbonate solution (50 mL). After drying over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure. The residue was purified by chromatography on a silica gel (25 g) column using hexane:ethyl acetate (7:2) as the eluant to give 1-fluoro-2-(4-nitrophenyl)ethane (359 mg).

후처리

  1. customto rise back to room temperature
  2. washThe methylene chloride solution was washed with saturated aqueous sodium hydrogen carbonate solution (50 mL)
  3. dry with materialAfter drying over anhydrous magnesium sulfate
  4. customthe solvent was evaporated under reduced pressure
  5. customThe residue was purified by chromatography on a silica gel (25 g) column

출처 및 근거

ORD 기록
ord-797e93aa1ccb49db8a3e3ff7a245dcc9
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07157442B2

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