Reaktion #1705967

ord-40d0ca85abcd4dffb1c1973d48e6be44

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe ice bath was removed
  2. 2
    workup.STIRRINGthe solution was stirred at rt for 3 h
  3. 3
    workup.ADDITIONThe reaction was poured into 2N HCl aqueous solution
  4. 4
    Extraktionextracted with EtOAc
  5. 5
    TrocknenThe combined organic extracts were dried over MgSO4
  6. 6
    Einengenconcentrated under reduced pressure

Vorschrift

To an ice cooled solution of 6-bromo-1,2-dihydrospiro[indole-3,3′-thietane] (0.25 g, 0.96 mmol), 4-dimethylaminopyridine (5.89 mg, 0.048 mmol), and triethylamine (0.269 mL, 1.928 mmol) in DCM (9.64 mL) was added acetyl chloride (0.137 mL, 1.928 mmol). The solution was stirred for 5 min at this temperature, the ice bath was removed and the solution was stirred at rt for 3 h. The reaction was poured into 2N HCl aqueous solution and extracted with EtOAc. The combined organic extracts were dried over MgSO4 and concentrated under reduced pressure to give 1-acetyl-6-bromo-1,2-dihydrospiro[indole-3,3′-thietane] as a yellow solid. Mass Spectrum (ESI) m/e=297.9 [(M+1) (79Br)] and 300.0 [(M+1) (81Br)].

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08765940B2uspto-grants-2014_07