Reaktion #2254154
ord-8cd3830461cc476896c7180c97132376
Reaktionsgleichung
S,S-Diisopropyl-S-aminosulfonium 2,4,6-trimethyl-phenylsulfonate
6,8-dichloro-1H-benzo[d][1,3]oxazine-2,4-dione
Water
potassium tert-butanolate
→
title compound
2-amino-N-(bis-2-propyl-λ4-sulfanylidene)-3,5-dichloro-benzamide
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigeto come to room temperature
- 2Sonstigethe organic phase was separated
- 3Extraktionthe aqueous phase further extracted with methylene chloride (2×100 mL)
- 4TrocknenThe combined organic extracts were dried (MgSO4)
- 5Einengenconcentrated in vacuo
Vorschrift
To a suspension of 6,8-dichloro-1H-benzo[d][1,3]oxazine-2,4-dione (45.0 g, 70.7 mmol) in methylene chloride (500 mL) was added S,S-Diisopropyl-S-aminosulfonium 2,4,6-trimethyl-phenylsulfonate (77.6 g, 234 mmol). The reaction mixture was cooled to 0° C. and potassium tert-butanolate (8.73 g, 77.8 mmol) was added after which the reaction was allowed to come to room temperature and stirred for 16 h. Water (200 mL) and methylene chloride (50 mL) were then added, the organic phase was separated and the aqueous phase further extracted with methylene chloride (2×100 mL). The combined organic extracts were dried (MgSO4) and concentrated in vacuo to afford the title compound (62.8 g, quant.).