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Ethyl trifluoroacetate → 1-(3,5-Dichloro-2,4-difluorophenyl)-2,2,2-trifluoroethanone

HRID 1500197
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1500197
[Cl:1][C:2]1[CH:7]=[C:6](I)[C:5]([F:9])=[C:4]([Cl:10])[C:3]=1[F:11].C([Mg]Cl)(C)C.[F:17][C:18]([F:25])([F:24])[C:19](OCC)=[O:20]>O1CCCC1.COC(C)(C)C>[Cl:10][C:4]1[C:5]([F:9])=[C:6]([C:19](=[O:20])[C:18]([F:25])([F:24])[F:17])[CH:7]=[C:2]([Cl:1])[C:3]=1[F:11]
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Komponenten

6

Edukt 3

HCID 9794Ethyl trifluoroacetateHCID 871589861,3-Dichloro-2,4-difluoro-5-iodobenzeneHCID 178418918HCID 178418918, Verbindung

Produkt 1

HCID 871586251-(3,5-Dichloro-2,4-difluorophenyl)-2,2,2-trifluoroethanoneAusbeute 69,2 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8028TetrahydrofuranLösungsmittel3×
HCID 15413tert-Butyl methyl etherLösungsmittel

Versuchsvorschrift

1,3-Dichloro-2,4-difluoro-5-iodobenzene (4.0 g) was dissolved in tetrahydrofuran and cooled to −10 degree. A 2.0 M solution of isopropylmagnesium chloride in tetrahydrofuran (10 ml) was added dropwise via a dropping funnel. The reaction mixture was stirred for 1 hour at same temperature. A solution of ethyl trifluoroacetate (2.76 g) in tetrahydrofuran (6 ml) was added dropwise and the reaction mixture was allowed to warm to ambient temperature. The reaction mixture was diluted with t-butyl methyl ether and washed with 1 N NaOH and then brine. The combined extracts were dried over magnesium sulfate. After filtered off, the filtrate was concentrated in vacuo to give crude product which was purified with Kugel-Rohr to give 1-(3,5-dichloro-2,4-difluorophenyl)-2,2,2-trifluoroethanone (2.5 g).

Aufarbeitung

  1. temperaturecooled to −10 degree
  2. washwashed with 1 N NaOH
  3. dry with materialThe combined extracts were dried over magnesium sulfate
  4. filtrationAfter filtered off
  5. concentrationthe filtrate was concentrated in vacuo
  6. customto give crude product which
  7. customwas purified with Kugel-Rohr

Quellen und Nachweise

ORD-Eintrag
ord-fc999ebbfbc040319171cf64ddba7a37
Quelldatensatz
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09206122B2

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