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Propargyl bromide → 6-(3-[1,3]Dioxan-2-ylphenyl)-6-methyl-4-trifluoromethylhept-1-yn-4-ol

HRID 400660
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 400660
[Al].[CH2:2](Br)[C:3]#[CH:4].[O:6]1[CH2:11][CH2:10][CH2:9][O:8][CH:7]1[C:12]1[CH:13]=[C:14]([C:18]([CH3:27])([CH3:26])[CH2:19][C:20](=[O:25])[C:21]([F:24])([F:23])[F:22])[CH:15]=[CH:16][CH:17]=1>C1COCC1.C(OCC)C>[O:6]1[CH2:11][CH2:10][CH2:9][O:8][CH:7]1[C:12]1[CH:13]=[C:14]([C:18]([CH3:27])([CH3:26])[CH2:19][C:20]([C:21]([F:23])([F:24])[F:22])([OH:25])[CH2:4][C:3]#[CH:2])[CH:15]=[CH:16][CH:17]=1
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Komponenten

6

Edukt 3

HCID 7842Propargyl bromideHCID 5359268AluminumHCID 578099664-(3-[1,3]Dioxan-2-ylphenyl)-1,1,1-trifluoro-4-methylpentan-2-one

Produkt 1

HCID 600268426-(3-[1,3]Dioxan-2-ylphenyl)-6-methyl-4-trifluoromethylhept-1-yn-4-olAusbeute 50 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 3283Diethyl EtherLösungsmittel
HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

Aluminum amalgam was prepared from aluminum foil (1.16 g, 14.4 mmol) and mercuric chloride (12 mg, catalytic amount) in 20 mL of anhydrous THF by vigorously stirring the mixture at room temperature for 1 hour under an argon atmosphere. A solution of propargyl bromide (4.80 mL, 80 wt. % in toluene, 43.1 mmol) in 25 mL of anhydrous THF was slowly added to a stirred suspension maintaining a temperature of 30° C.-40° C., and after addition, stirring at 40° C. was continued until a dark gray solution was obtained (ca. 1 hour). The propargyl aluminum sesquibromide solution was added to a solution of 4-(3-[1,3]dioxan-2-ylphenyl)-1,1,1-trifluoro-4-methylpentan-2-one (5.6 g, 14.2 mmol) in 100 mL of anhydrous diethyl ether at −78° C. The reaction mixture was stirred at this temperature for 3 hours, and then was allowed to warm to room temperature, at which time it was stirred for 12 hours. The reaction mixture was then poured into 20 mL of ice-water and extracted with four 30 mL portions of diethyl ether. The combined extracts were washed with 20 mL of brine, dried over magnesium sulfate, and concentrated in vacuo. Chromatography on silica gel (100% hexanes to 40% ethyl acetate in hexanes, gradient) afforded 2.5 g of the title compound as an oil (50% yield).

Aufarbeitung

  1. temperaturemaintaining a temperature of 30° C.-40° C.
  2. additionafter addition
  3. stirringstirring at 40° C.
  4. customwas obtained (ca. 1 hour)
  5. stirringThe reaction mixture was stirred at this temperature for 3 hours
  6. temperatureto warm to room temperature, at which time it
  7. stirringwas stirred for 12 hours
  8. extractionextracted with four 30 mL portions of diethyl ether
  9. washThe combined extracts were washed with 20 mL of brine
  10. dry with materialdried over magnesium sulfate
  11. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-f75e3933080644f7af7056de36b77a7b
Quelldatensatz
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08741897B2

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