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Pyridine → Trifluoroethyl 3-methoxytetrafluoropropionate

HRID 482822
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HRID 482822 반응식
[CH3:1][O:2][C:3]([F:11])([F:10])[C:4]([F:9])([F:8])[C:5](Cl)=[O:6].[CH2:12]([OH:17])[C:13]([F:16])([F:15])[F:14].N1C=CC=CC=1>C(Cl)Cl>[CH3:1][O:2][C:3]([F:11])([F:10])[C:4]([F:9])([F:8])[C:5]([O:17][CH2:12][C:13]([F:16])([F:15])[F:14])=[O:6]
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참가 물질

5

반응물 3

HCID 1049Pyridine2회HCID 64092,2,2-TrifluoroethanolHCID 128460263-Methoxy-2,2,3,3-tetrafluoropropionyl chloride

생성물 1

HCID 13571089Trifluoroethyl 3-methoxytetrafluoropropionate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Trifluoroethyl 3-methoxytetrafluoropropionate was prepared by reaction of 97.3 g (0.50 mol) of 3-methoxytetrafluoropropionyl chloride, 55.0 g (0.55 mol) of trifluoroethanol, and 39.5 g (0.50 mol) of pyridine in 100 mL methylene chloride. Reaction was extremely slow until the pyridine was added. After having stirred overnight, the reaction mixture was filtered, solids were rinsed with methylene chloride, and filtrates were distilled to give 119.4 g of ester, bp 44°-49° (20 mm, 2.7 kPa). The cloudy product was treated with 2 g of P2O5 and filtered to afford 109.3 g (93%) of the desired ester, pure by GC. IR (CCl4): 2855, 2975, and 3010 (sat'd CH), 1790 (C=O), and 1300-1100 cm-1 (CF, C--O).

후처리

  1. customReaction
  2. additionwas added
  3. filtrationthe reaction mixture was filtered
  4. washsolids were rinsed with methylene chloride, and filtrates
  5. distillationwere distilled

출처 및 근거

ORD 기록
ord-0b5c246ecb1442b1a3041dc937604888
출처 데이터셋
uspto-grants-1986_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04576752

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