Ethanol → 2,3,4,6-Tetrafluorobenzoic acid ethyl ester

HRID 729358노트

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HRID 729358 반응식
[F:1][C:2]1[C:10]([F:11])=[C:9]([F:12])[CH:8]=[C:7]([F:13])[C:3]=1[C:4]([OH:6])=[O:5].[C:14](Cl)(=O)[C:15](Cl)=O.C(O)C.C([O-])(O)=O.[Na+]>ClCCl.CN(C)C=O.C1C=CC=CC=1>[CH2:14]([O:5][C:4](=[O:6])[C:3]1[C:7]([F:13])=[CH:8][C:9]([F:12])=[C:10]([F:11])[C:2]=1[F:1])[CH3:15]

참가 물질

8

반응물 4

HCID 702EthanolHCID 65578Oxalyl chlorideHCID 516892Sodium BicarbonateHCID 27765912,3,4,6-tetrafluorobenzoic Acid

생성물 1

HCID 210411752,3,4,6-Tetrafluorobenzoic acid ethyl ester수율 60.1%

시약·촉매·용매 3

HCID 6228Dimethylformamide촉매HCID 241Benzene용매HCID 6344Dichloromethane용매2회

실험 절차

2,3,4,6-Tetrafluorobenzoic acid (4.8 g, 24.7 mmol) in dichloromethane (80 mL) is cooled to 0° C. under a nitrogen atmosphere and treated with oxalyl chloride (11.2 mL, 128 mmol) followed by anhydrous N,N-dimethylformamide (2 drops). The mixture is warmed to room temperature and stirred for 2 hours. The solution is co-evaporated with benzene to yield an oil that is taken up in dichloromethane (80 mL), cooled to 0° C. under an inert atmosphere, and treated with anhydrous ethanol (15 mL, 258 mmol). After 5 hours at room temperature, the solution is poured into saturated NaHCO3 and extracted with chloroform. The organic phase is washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum to provide the title compound (3.3 g). This material is used without further purification. 1H NMR (CDCl3): δ 6.93-6.75 (m, 1H), 4.42 (q, 2H), 1.39 (t, 3H).

후처리

  1. customto yield an oil that
  2. temperaturecooled to 0° C. under an inert atmosphere
  3. waitAfter 5 hours at room temperature
  4. extractionextracted with chloroform
  5. washThe organic phase is washed with brine
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-3b35c986c6404776ae92641734cd98ea
출처 데이터셋
uspto-grants-2009_09
특허 번호
US07582627B2

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