Dimethyl Sulfoxide → 2-(2,4-Dichlorophenyl)-2-methyloxirane

HRID 1400348

Reaktionsgleichung

Reaktionsgleichung von HRID 1400348
CS(C)=O.[H-].[Na+].[I-].[CH3:8][S+](C)C.[Cl:12][C:13]1[CH:18]=[C:17]([Cl:19])[CH:16]=[CH:15][C:14]=1[C:20](=[O:22])[CH3:21]>C1COCC1>[Cl:12][C:13]1[CH:18]=[C:17]([Cl:19])[CH:16]=[CH:15][C:14]=1[C:20]1([CH3:8])[CH2:21][O:22]1

Komponenten

6

Edukt 4

HCID 679Dimethyl SulfoxideHCID 166932',4'-DichloroacetophenoneHCID 24758Sodium hydrideHCID 75127Trimethylsulfonium iodide

Produkt 1

HCID 199924372-(2,4-Dichlorophenyl)-2-methyloxirane

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

DMSO is added to NaH (1-1.8 equiv.) and heated to 65° C. for one h. THF is added at same temperature and heated for another 10 min. After 10 min., the reaction mixture is cooled to 0° C. Trimethylsulfonium iodide (1-1.2 equiv.) is added and the contents are stirred for 10 min. after which the solution of 1-(2,4-dichlorophenyl)ethanone (1 equiv.) in THF is added dropwise. After complete addition, the reaction mixture is stirred at RT for 2 h; the reaction is monitored by LCMS. After completion, the reaction mixture is poured in ice water, extracted in diethyl ether, dried over sodium sulfate and concentrated at 25° C. to get the crude product.

Aufarbeitung

  1. temperatureheated for another 10 min
  2. temperaturethe reaction mixture is cooled to 0° C
  3. additionis added dropwise
  4. additionAfter complete addition
  5. extractionextracted in diethyl ether
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated at 25° C.

Quellen und Nachweise

ORD-Eintrag
ord-71b63768a2b848828732a6cd03ed44f1
Quelldatensatz
uspto-grants-2014_12
Patentnummer
US08906925B2

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