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5-Chloro-2-methoxyaniline → 5-Chloro-2-methoxy-beta-[3,5-bis(trifluoromethyl)phenyl]styrene

HRID 644458
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 644458
N([O-])=O.[Na+].N[C:6]1[CH:11]=[C:10]([Cl:12])[CH:9]=[CH:8][C:7]=1[O:13][CH3:14].[F:15][C:16]([F:30])([F:29])[C:17]1[CH:18]=[C:19]([CH:22]=[C:23]([C:25]([F:28])([F:27])[F:26])[CH:24]=1)[CH:20]=[CH2:21]>O.[H+].[B-](F)(F)(F)F.CO.C(OCC)(=O)C>[Cl:12][C:10]1[CH:9]=[CH:8][C:7]([O:13][CH3:14])=[C:6]([CH:11]=1)[CH:21]=[CH:20][C:19]1[CH:22]=[C:23]([C:25]([F:26])([F:28])[F:27])[CH:24]=[C:17]([C:16]([F:15])([F:29])[F:30])[CH:18]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 3

HCID 667635-Chloro-2-methoxyanilineHCID 27732423,5-Bis(trifluoromethyl)styreneHCID 23668193Sodium Nitrite

Produkt 1

HCID 765461385-Chloro-2-methoxy-beta-[3,5-bis(trifluoromethyl)phenyl]styreneAusbeute 34,7 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 887MethanolLösungsmittel
HCID 962
Water
Lösungsmittel
HCID 8857Ethyl AcetateLösungsmittel
HCID 28118Tetrafluoroboric acidLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A solution of sodium nitrite (57 mg, 0.8 mmol) in water (1 mL) was added to a solution of 2-amino-4-chloroanisole (131 mg, 0.8 mmol) in 48% hydrogen tetrafluoroborate (0.3 mL) under ice cooling and argon atmosphere. After the mixture was stirred at 0° C. for 1 hour, a solution of 3,5-bis(trifluoromethyl)styrene (100 mg, 0.4 mmol) in methanol (3 mL) was added and the mixture was stirred at 50° C. for 1 hour. After the reaction mixture was cooled to room temperature, the residue obtained by evaporation of the solvent under reduced pressure was diluted with ethyl acetate. After the solution was washed successively with 2N hydrochloric acid, water and brine, dried over anhydrous sodium sulfate, the residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1) to give the title compound (52.8 mg, 33.3%) as a white powder.

Aufarbeitung

  1. stirringthe mixture was stirred at 50° C. for 1 hour
  2. temperatureAfter the reaction mixture was cooled to room temperature
  3. customthe residue obtained by evaporation of the solvent under reduced pressure
  4. washAfter the solution was washed successively with 2N hydrochloric acid, water and brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. customthe residue obtained by evaporation of the solvent under reduced pressure
  7. customwas purified by column chromatography on silica gel (n-hexane:ethyl acetate=5:1)

Quellen und Nachweise

ORD-Eintrag
ord-84c38d26b4db498692231614c5f962f7
Quelldatensatz
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07700655B2

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