1,3-Dichloroacetone → 2-tert-Butyl-4-(chloromethyl)-1,3-oxazole

HRID 1357432Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1357432
[C:1]([NH2:7])(=[O:6])[C:2]([CH3:5])([CH3:4])[CH3:3].[Cl:8][CH2:9][C:10](=O)[CH2:11]Cl.[OH-].[Na+]>>[C:2]([C:1]1[O:6][CH:11]=[C:10]([CH2:9][Cl:8])[N:7]=1)([CH3:5])([CH3:4])[CH3:3]

Komponenten

4

Edukt 3

HCID 107931,3-DichloroacetoneHCID 12957TrimethylacetamideHCID 14798Sodium Hydroxide

Produkt 1

HCID 221695102-tert-Butyl-4-(chloromethyl)-1,3-oxazoleAusbeute 51,2 %

Reaktionsbedingungen

Temperatur
135 °C

Versuchsvorschrift

25 g of pivalic acid amide and 25 g of 1,3-dichloro-2-propanone were mixed and heated on an oil bath at 135° C. for 2.5 hours. After having been cooled with ice, the mixture was made alkaline with an aqueous solution of sodium hydroxide added thereto. Then, the resulting product was extracted with ethyl acetate, washed with water, and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residual product was purified through column chromatography (silica gel; ethyl acetate n-hexane=1:8) to obtain 17.5 g of 2-tert-butyl-4-chloromethyloxazole.

Aufarbeitung

  1. temperatureAfter having been cooled with ice
  2. additionadded
  3. extractionThen, the resulting product was extracted with ethyl acetate
  4. washwashed with water
  5. dry with materialdried over anhydrous sodium sulfate
  6. distillationthe solvent was distilled off under reduced pressure
  7. customThe residual product was purified through column chromatography (silica gel; ethyl acetate n-hexane=1:8)

Quellen und Nachweise

ORD-Eintrag
ord-bf21c0f21a2447efbae42923a172a5bd
Quelldatensatz
uspto-grants-2003_07
Patentnummer
USRE038188E1

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