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Chlorodifluoromethane → 1,3-Dibromo-5-(difluoromethoxy)benzene

HRID 1990745
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1990745
[Br:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[C:6]([Br:8])[CH:7]=1.Cl[CH:11]([F:13])[F:12]>CC(O)C.[OH-].[K+].O>[Br:1][C:2]1[CH:3]=[C:4]([O:9][CH:11]([F:13])[F:12])[CH:5]=[C:6]([Br:8])[CH:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 2

HCID 6372Chlorodifluoromethane2×HCID 122803,5-Dibromophenol

Produkt 1

HCID 219046401,3-Dibromo-5-(difluoromethoxy)benzeneAusbeute 80 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962WaterLösungsmittelHCID 3776IsopropanolLösungsmittel
HCID 14797
Potassium Hydroxide
Lösungsmittel

Versuchsvorschrift

To a tared, sealed 350 mL round-bottomed pressure flask containing a solution of 3,5-dibromophenol (10.0 g, 39.7 mmol; see Example 27(ii) above) in 2-propanol (100 mL) and 30% KOH (80 mL) at −78° C. was added chlorodifluoromethane via bubbling for 15 min through the septum. The septum was replaced with a Teflon stopper and the flask was then sealed and allowed to warm to room temperature where the flask was weighed and determined to contain 12.0 g (138 mmol) of chlorodifluoromethane. The solution was refluxed overnight in an oil bath set at 80° C. The flask was cooled to room temperature, the pressure cautiously released and the contents diluted with H2O (200 mL). The aqueous layer was extracted with CHCl3 (2× 150 mL), then the combined organics were dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by Kugelrohr distillation at 80° C. at 0.2 mm Hg to afford the sub-title compound (9.6 g, 80%) as clear liquid.

Aufarbeitung

  1. customsealed 350 mL round-bottomed pressure flask
  2. customvia bubbling for 15 min through the septum
  3. customthe flask was then sealed
  4. temperatureThe solution was refluxed overnight in an oil bath
  5. customset at 80° C
  6. temperatureThe flask was cooled to room temperature
  7. extractionThe aqueous layer was extracted with CHCl3 (2× 150 mL)
  8. dry with materialthe combined organics were dried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo
  11. distillationThe residue was purified by Kugelrohr distillation at 80° C. at 0.2 mm Hg

Quellen und Nachweise

ORD-Eintrag
ord-843aeb5cdf1546fbba764d48922a7741
Quelldatensatz
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07645751B2

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