Reaktion #94173

ord-c0ea7a63904b4208a7358325c5e032b5

Reaktionsgleichung

O=O
oxygen
CC(C)(C)OO
t-butyl hydroperoxide
[Na+].[OH-]
sodium hydroxide
Cc1ccc(OC(=O)CCC(=O)Cl)cc1
3-(p-tolyloxycarbonyl)propionyl chloride
Cc1ccc(OC(=O)CCC(=O)OOC(C)(C)C)cc1
t-Butyl O-p-Tolyl Monoperoxysuccinate
Ausbeute 92.8%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenthe resulting ether solution was washed, first with 10% sodium hydroxide solution
  2. 2
    TrocknenAfter drying over anhydrous MgSO4 and removal of the ether in vacuo 28.2 g
  3. 3
    Sonstige(theory, 30.4 g.) of white solid, m.p. 72°-77° C., was obtained

Vorschrift

To a vigorously stirred solution of 15.6 g. (0.143 mole) of 82.0% t-butyl hydroperoxide and 57.0 g. (0.143 mole) of aqueous 10% sodium hydroxide at 5°-10° C. was added slowly 24.6 g. (0.109 mole) of 3-(p-tolyloxycarbonyl)propionyl chloride (prepared from p-tolyl 3-carboxypropionate and thionyl chloride) in 50 ml. of diethyl ether. The reaction mixture was then stirred at 5°-10° C. for 3 hours, after which additional ether was added to the mixture and the resulting ether solution was washed, first with 10% sodium hydroxide solution, and finally with water until the solution was neutral. After drying over anhydrous MgSO4 and removal of the ether in vacuo 28.2 g. (theory, 30.4 g.) of white solid, m.p. 72°-77° C., was obtained. The assay according to "active oxygen" content was 100% and the corrected yield was 92.8%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04129586uspto-grants-1978_12