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Water → 4-Bromomethyl-5-methyl-3-trifluoromethylisoxazole

HRID 1172119
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1172119
[CH3:1][C:2]1[O:6][N:5]=[C:4]([C:7]([F:10])([F:9])[F:8])[C:3]=1[CH2:11]O.P(Br)(Br)[Br:14].O>C(OCC)C>[Br:14][CH2:11][C:3]1[C:4]([C:7]([F:10])([F:9])[F:8])=[N:5][O:6][C:2]=1[CH3:1]
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Komponenten

5

Edukt 3

HCID 962WaterHCID 24614Phosphorus tribromideHCID 17862894(5-Methyl-3-trifluoromethylisoxazol-4-yl)-methanol

Produkt 1

HCID 178628854-Bromomethyl-5-methyl-3-trifluoromethylisoxazoleAusbeute 82 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Versuchsvorschrift

A solution of 0.45 g (2.5 mmoles) of (5-methyl-3-trifluoromethylisoxazol-4-yl)-methanol dissolved in 10 ml of diethyl ether was cooed to 0° C. Thereto was added 0.2 g (8.9 mmoles) of phosphorus tribromide. The mixture was stirred at room temperature for 1 hour to give rise to a reaction. After the completion of the reaction, the reaction mixture was poured into water, followed by extraction with diethyl ether. The resulting organic layer was washed with an aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein, to obtain 0.5 g (yield: 74.0%) of 4-bromomethyl-5-methyl-3-trifluoromethylisoxazole.

Aufarbeitung

  1. customwas cooed to 0° C
  2. customto give rise
  3. customto a reaction
  4. customAfter the completion of the reaction
  5. extractionfollowed by extraction with diethyl ether
  6. washThe resulting organic layer was washed with an aqueous sodium chloride solution
  7. dry with materialdried over anhydrous magnesium sulfate
  8. distillationThe resulting solution was subjected to vacuum distillation
  9. customto remove the solvent

Quellen und Nachweise

ORD-Eintrag
ord-0157d62e35264bd4bbb7bf877828ed18
Quelldatensatz
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07833939B2

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