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Tetrahydrofuran → 5-Acetyl-5-methyl-1,3-dioxan-2-one

HRID 376495
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 376495
Cl[C:2](Cl)([O:4][C:5](=[O:11])[O:6][C:7](Cl)(Cl)Cl)Cl.O[CH2:14][C:15](CO)(C)[C:16](=[O:18])[CH3:17].C1COCC1>C(N(CC)CC)C>[C:16]([C:15]1([CH3:14])[CH2:7][O:6][C:5](=[O:11])[O:4][CH2:2]1)(=[O:18])[CH3:17]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 8028TetrahydrofuranHCID 94429TriphosgeneHCID 5365163,3-Bis(hydroxymethyl)-2-butanone

Produkt 1

HCID 219992315-Acetyl-5-methyl-1,3-dioxan-2-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8471TriethylamineLösungsmittel

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

In a one liter three neck flask equipped with a mechanical stirrer and under nitrogen were added triphosgene (37.0 g), 3,3-dihydroxymethyl-2-butanone (50 g) and THF (300 mL). The resulting mixture was stirred until a homogeneous solution resulted. This homogeneous solution was cooled to -78° C. Triethylamine (75.0 g) was added to the this solution over 30 min. The cold bath was removed and the reaction allowed to warm to room temperature. After stirring for one hour at room temperature the triethylamine/HCl salt was removed by filtration and the filtrate pass through a silica gel plug. The solvent was removed under reduced pressure resulting in an off white product. This product was then washed with hot ether giving a white solid. NMR analysis indicated that the product contained a small amount of triethylamine/HCl salt, thus the material was dissolved in dichloromethane and washed with water affording 15.02 g of material. 1H NMR (CDCl3) ppm: 4.70 (ab doublet, 2H), 4.20 (ab doublet, 2H), 2.3 (S, 3H), 1.25 (S, 3H).

Aufarbeitung

  1. customresulted
  2. customThe cold bath was removed
  3. temperatureto warm to room temperature
  4. stirringAfter stirring for one hour at room temperature the triethylamine/HCl salt
  5. customwas removed by filtration
  6. customThe solvent was removed under reduced pressure
  7. customresulting in an off white product
  8. washThis product was then washed with hot ether giving a white solid
  9. dissolutionthus the material was dissolved in dichloromethane
  10. washwashed with water affording 15.02 g of material

Quellen und Nachweise

ORD-Eintrag
ord-99eca2c39b55410782602a39a85cce62
Quelldatensatz
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06020499

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