Reaktion #50422

ord-0b48dd619f2a4b93b2a672614333945e

Reaktionsgleichung

CC(C)(C)[O-].[K+]
Potassium t-butoxide
CCOC=O
Ethyl formate
CCCC(=O)c1cccc2c1CC(N(CCC)CCC)CC2
2-di-n-propylamino-8-butyryl-1,2,3,4-tetrahydronaphthalene
C1CCOC1
THF
[NH4+].[OH-]
ammonium hydroxide
NO
Hydroxylamine
C1CCOC1
tetrahydrofuran
CCCN(CCC)C1CCc2cccc(-c3oncc3CC)c2C1
2-Di-n-propylamino-8-(4-ethylisoxazol-5-yl)-1,2,3,4-tetrahydronaphthalene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.DISSOLUTIONto dissolve the solid
  2. 2
    workup.STIRRINGwas stirred at room temperature for 20 hours after which it
  3. 3
    ExtraktionThe mixture was then extracted with methylene chloride
  4. 4
    TrocknenThe extract was dried over sodium sulfate
  5. 5
    Sonstigeevaporated
  6. 6
    workup.DISSOLUTIONThe residue was dissolved in 100 of toluene, and 100 mg of p-toluenesulfonic acid
  7. 7
    workup.ADDITIONwas added
  8. 8
    TemperaturThe mixture then was refluxed for 1.5 hours after which it
  9. 9
    workup.ADDITIONwas poured into water
  10. 10
    Extraktionextracted with methylene chloride
  11. 11
    ExtraktionThe methylene chloride extract
  12. 12
    Trocknenwas dried over sodium sulfate
  13. 13
    Sonstigeevaporated

Vorschrift

Potassium t-butoxide (0.82 g; 7.3 mmol) was suspended in 100 ml of tetrahydrofuran (THF). Ethyl formate (1.0 g; 13.3 mmol) and 2-di-n-propylamino-8-butyryl-1,2,3,4-tetrahydronaphthalene (1.0 g; 3.3 mmol) in THF was added to the mixture. The resulting mixture was stirred at room temperature overnight. Hydroxylamine (1.2 g; 16.6 mmol) was added followed by sufficient water to dissolve the solid. The resulting mixture, having pH 6, was stirred at room temperature for 20 hours after which it was poured into water, and the pH was adjusted to 12 with ammonium hydroxide. The mixture was then extracted with methylene chloride. The extract was dried over sodium sulfate and evaporated. The residue was dissolved in 100 of toluene, and 100 mg of p-toluenesulfonic acid was added. The mixture then was refluxed for 1.5 hours after which it was poured into water and extracted with methylene chloride. The methylene chloride extract was dried over sodium sulfate and evaporated.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05426226uspto-grants-1995_06