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p-Toluenesulfonic acid → 2-(4-Bromo-2,6-dimethylphenyl)-1,3-dioxane

HRID 1177406
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1177406
[Br:1][C:2]1[CH:9]=[C:8]([CH3:10])[C:5]([CH:6]=[O:7])=[C:4]([CH3:11])[CH:3]=1.CC1C=CC(S(O)(=O)=O)=CC=1.[CH2:23](O)[CH2:24][CH2:25][OH:26].CCCCCC>C1(C)C=CC=CC=1>[Br:1][C:2]1[CH:3]=[C:4]([CH3:11])[C:5]([CH:6]2[O:26][CH2:25][CH2:24][CH2:23][O:7]2)=[C:8]([CH3:10])[CH:9]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6101p-Toluenesulfonic acidHCID 8058HexaneHCID 104421,3-PropanediolHCID 110202224-Bromo-2,6-dimethylbenzaldehyde

Produkt 1

HCID 591748982-(4-Bromo-2,6-dimethylphenyl)-1,3-dioxane

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140Toluene
Lösungsmittel

Reaktionsbedingungen

Temperatur
140 °C

Versuchsvorschrift

A mixture of 4-bromo-2,6-dimethylbenzaldehyde (2.51 g, 12 mmol), 4-methyl-benzenesulfonic acid (0.20 g, 1.2 mmol), and propane-1,3-diol (1.2 mL, 16 mmol) in toluene (200 mL) was heated under nitrogen at 140° C. for 16 h, using a Dean-Stark trap to remove water. The reaction solution was then cooled to 25° C., diluted with EtOAc (200 mL), and sequentially washed with saturated aqueous sodium bicarbonate solution (100 mL) and brine (100 mL). The organic layer was separated, dried over MgSO4, filtered, and concentrated in vacuo to provide a yellow-brown oil. Hexane (200 mL) was added to the oil, and the resulting mixture was stirred vigorously for 10 min, resulting in the precipitation of a solid. This solid was collected by vacuum filtration, washed with hexanes (100 mL), and dried in vacuo to provide 2-(4-bromo-2,6-dimethylphenyl)-1,3-dioxane as a tan solid.

Aufarbeitung

  1. customto remove water
  2. temperatureThe reaction solution was then cooled to 25° C.
  3. additiondiluted with EtOAc (200 mL)
  4. washsequentially washed with saturated aqueous sodium bicarbonate solution (100 mL) and brine (100 mL)
  5. customThe organic layer was separated
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customto provide a yellow-brown oil
  10. customresulting in the precipitation of a solid
  11. filtrationThis solid was collected by vacuum filtration
  12. washwashed with hexanes (100 mL)
  13. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-4637d778b57747399612fe8a89d9acbd
Quelldatensatz
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07842685B2

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