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Methyl iodide → 3-Methyl-5-[2-[(phenylmethyl)thio]phenyl]-1,3,4-oxadiazol-2(3H)-one

HRID 255824
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 255824
[CH3:1]C(C)([O-])C.[K+].[C:7]1([CH2:13][S:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[C:21]2[O:25][C:24](=[O:26])[NH:23][N:22]=2)[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.CI>CN(C=O)C>[CH3:1][N:23]1[N:22]=[C:21]([C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=2[S:14][CH2:13][C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[O:25][C:24]1=[O:26]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6328Methyl iodideHCID 139588535-{2-[(Phenylmethyl)thio]phenyl}-1,3,4-oxadiazol-2(3H)-oneHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 139588543-Methyl-5-[2-[(phenylmethyl)thio]phenyl]-1,3,4-oxadiazol-2(3H)-oneAusbeute 68,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

To a suspension of 2.9 g of potassium t-butoxide in 60 ml of DMF under a N2 atmosphere was added portionwise 7 g of the product of Example 1 while maintaining the reaction temperature at 25°-30° C. with an ice-water bath. After stirring at 25° C. for 1 hour, 7 g of methyl iodide was added dropwise to cause an exotherm to 37° C. The suspension was heated at 40°-60° C. for 5 hours, then cooled to 25° and poured onto excess ice-water to yield a precipitate. The suspension was filtered, and the isolated solid was dissolved in tetrahydrofuran and dried over MgSO4. The isolated solid was passed through a silica gel column with methylene chloride and, after evaporation of the first eluant, 5 g of the subject compound was obtained; m.p. 137°-140° C.

Aufarbeitung

  1. temperaturewhile maintaining the reaction temperature at 25°-30° C. with an ice-water bath
  2. customto 37° C
  3. temperatureThe suspension was heated at 40°-60° C. for 5 hours
  4. temperaturecooled to 25°
  5. customto yield a precipitate
  6. filtrationThe suspension was filtered
  7. dissolutionthe isolated solid was dissolved in tetrahydrofuran
  8. dry with materialdried over MgSO4
  9. customafter evaporation of the first eluant

Quellen und Nachweise

ORD-Eintrag
ord-a0fbf1951fcb44e4b5b2b3b7c1e13f43
Quelldatensatz
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04699647

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