Diisopropylethylamine → 3-(2,3-Dihydro-2,2,4-trimethylbenzofuran-7-yl)-5-(methylamino)-1,3,4-oxadiazol-2(3H)-one

HRID 1583756Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1583756
[CH3:1][C:2]1([CH3:22])[CH2:6][C:5]2[C:7]([CH3:21])=[CH:8][CH:9]=[C:10]([N:11]3[N:15]=[C:14]([N:16](OC)[CH3:17])[O:13][C:12]3=[O:20])[C:4]=2[O:3]1.C(N(C(C)C)CC)(C)C>CO>[CH3:1][C:2]1([CH3:22])[CH2:6][C:5]2[C:7]([CH3:21])=[CH:8][CH:9]=[C:10]([N:11]3[N:15]=[C:14]([NH:16][CH3:17])[O:13][C:12]3=[O:20])[C:4]=2[O:3]1

Komponenten

4

Versuchsvorschrift

A solution of 3.0 g of 3, 75 ml of methanol and 1.3 g of N,N-diisopropyl-N-ethylamine was warmed on a steam bath for 18 hours. The solvent was evaporated under reduced pressure, the residue was mixed with 75 ml of water and the mixture was extracted with ether. The extract was dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was flash-chromatographed over silica gel, using a 2:15:33 v:v:v mixture of THF, ethyl acetate and hexane as eluent. Two products were obtained: one, a light amber syrup, Rf=0.49, was identified as 3; the second, a solid (Rf=0.24) was recrystallized from ether to give 4, as a colorless solid, m.p.: 183°-184° C.

Aufarbeitung

  1. customThe solvent was evaporated under reduced pressure
  2. additionthe residue was mixed with 75 ml of water
  3. extractionthe mixture was extracted with ether
  4. dry with materialThe extract was dried (MgSO4)
  5. customthe solvent was evaporated under reduced pressure
  6. customThe residue was flash-chromatographed over silica gel
  7. additionv:v mixture of THF, ethyl acetate and hexane as eluent
  8. customTwo products were obtained
  9. customthe second, a solid (Rf=0.24) was recrystallized from ether
  10. customto give 4

Quellen und Nachweise

ORD-Eintrag
ord-83cce786075840d9a41a9854b1b39dee
Quelldatensatz
uspto-grants-1985_11
Patentnummer
US04554283

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