Reacción #2254154
ord-8cd3830461cc476896c7180c97132376
Ecuación de reacción
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
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otroto come to room temperature
- 2Otrothe organic phase was separated
- 3Extracciónthe aqueous phase further extracted with methylene chloride (2×100 mL)
- 4SecadoThe combined organic extracts were dried (MgSO4)
- 5Concentraciónconcentrated in vacuo
Procedimiento
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.).