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3-(Trifluoromethyl)phenol → 2-Butanol, 1-[3-(trifluoromethyl)phenoxy]-

HRID 465271
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 465271
[F:1][C:2]([F:11])([F:10])[C:3]1[CH:4]=[C:5]([OH:9])[CH:6]=[CH:7][CH:8]=1.[O:12]1[CH:14]([CH2:15][CH3:16])[CH2:13]1.[OH-].[K+]>O>[F:1][C:2]([F:10])([F:11])[C:3]1[CH:4]=[C:5]([CH:6]=[CH:7][CH:8]=1)[O:9][CH2:13][CH:14]([OH:12])[CH2:15][CH3:16]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 73763-(Trifluoromethyl)phenolHCID 78341,2-Epoxybutane2×HCID 14797Potassium Hydroxide

Produkt 1

HCID 113793022-Butanol, 1-[3-(trifluoromethyl)phenoxy]-Ausbeute 95,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

A mixture of 3-trifluoromethylphenol (75 ml, 0.617 moles), 1,2-epoxybutane (58 ml, 0.617 moles), potassium hydroxide pellets (86%, 0.062 moles), and water (100 ml) were heated with stirring at 65° C. for four hours. At this point more 1,2-epoxybutane (58 ml, 0.617 moles) was added and stirring at 65° C. continued overnight. The reaction was allowed to cool to room temperature and the lower phase taken off and the upper phase extracted with methylene chloride (2×100 ml). The organic phases were combined and washed with 5% sodium hydroxide solution (150 ml) and water (3×150 ml). This reaction solution was dried over anhydrous magnesium sulfate and stripped under vacuo to yield 138 g of the desired alcohol, as determined by infra-red spectroscopy, mass spectrometry and nuclear magnetic resonance spectroscopy.

Aufarbeitung

  1. temperaturewere heated
  2. stirringstirring at 65° C.
  3. waitcontinued overnight
  4. temperatureto cool to room temperature
  5. extractionthe upper phase extracted with methylene chloride (2×100 ml)
  6. washwashed with 5% sodium hydroxide solution (150 ml) and water (3×150 ml)
  7. dry with materialThis reaction solution was dried over anhydrous magnesium sulfate

Quellen und Nachweise

ORD-Eintrag
ord-d0b65d578c22418ab8fa0b04e6fdedfa
Quelldatensatz
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05152827

Notizen zur Reaktion

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