Ethanol → Ethyl 2H-tetrafluorobenzoate

HRID 10268노트

반응식

HRID 10268 반응식
[F:1][C:2]1[C:10]([F:11])=[C:9]([F:12])[C:8]([F:13])=[CH:7][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>[CH2:14]([O:5][C:4](=[O:6])[C:3]1[CH:7]=[C:8]([F:13])[C:9]([F:12])=[C:10]([F:11])[C:2]=1[F:1])[CH3:15]

참가 물질

7

반응 조건

온도
0 °C

실험 절차

A solution of 2,3,4,5-tetrafluorobenzoic acid (4.68 g, 24.1 mmol) in dichloromethane (50 mL) at 0° C. is treated with oxalyl chloride (11.5 mL, 132 mmol) followed by N,N-dimethylformamide (4 drops). The mixture is stirred at 0° C. for 5 minutes and then at room temperature for 1.5 hours. The mixture is concentrated to dryness and subsequently co-evaporated from benzene. The resulting acid chloride is diluted with dichloromethane (50 mL), cooled to 0° C., and anhydrous ethanol (15.0 mL, 256 mmol) is added dropwise. The resulting solution is stirred at room temperature for 4.5 hours, then poured into saturated NaHCO3 and extracted with chloroform. The combined organic extracts are washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum to afford the title compound (5.37 g). 1H NMR (CDCl3): δ 7.67–7.55 (m, 1H), 4.42 (q, 2H), 1.41 (t, 3H).

후처리

  1. waitat room temperature for 1.5 hours
  2. concentrationThe mixture is concentrated to dryness
  3. additionThe resulting acid chloride is diluted with dichloromethane (50 mL)
  4. temperaturecooled to 0° C.
  5. stirringThe resulting solution is stirred at room temperature for 4.5 hours
  6. extractionextracted with chloroform
  7. washThe combined organic extracts are washed with brine
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-e23d6a74247b400bb87430ce70adc43b
출처 데이터셋
uspto-grants-2006_08
특허 번호
US07094780B1

반응 노트

불러오는 중…