Reacción #59262

ord-6983da0e423f4f0586daf65b5c99150f

Ecuación de reacción

O=C=NS(=O)(=O)Cl
chlorosulfonyl isocyanate
COc1ccc(N)cc1
4-methoxyaniline
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
COc1ccc2c(c1)S(=O)(=O)NC(=O)N2
desired product ( 8 )
Rendimiento 95.0%
COc1ccc2c(c1)S(=O)(=O)NC(=O)N2
7-Methoxy-1,1-dioxo-1,4-dihydro-2H-1λ6-benzo[1,2,4]thiadiazin-3-one
Rendimiento 95.0%

Condiciones de reacción

Temperatura
-40°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    workup.STIRRINGthe reaction was stirred for an additional 5 minutes
  3. 3
    TemperaturaThe mixture was then quickly heated to 110° C.
  4. 4
    workup.STIRRINGwith stirring for 20 minutes
  5. 5
    Filtraciónthe precipitate was collected by suction filtration
  6. 6
    Lavadowashed with cold water
  7. 7
    Otrodried in vacuo

Procedimiento

A solution of chlorosulfonyl isocyanate (17 mL, 195 mmol.) was dissolved in 150 mL of nitroethane and cooled to −40° C. A solution of 4-methoxyaniline (Z) (20 g, 162 mmol) in 100 mL of nitroethane was then added drop-wise from a dropper funnel with stirring. After the addition was completed, the reaction was stirred for an additional 5 minutes and aluminum chloride (25 g, 195 mmol) was added. The mixture was then quickly heated to 110° C. with stirring for 20 minutes. The crude material was then poured onto ice and the precipitate was collected by suction filtration, washed with cold water, and dried in vacuo to produce 35 g of the desired product (8) as a purple powder in 95% yield. 1H NMR (400 MHz, DMSO-d6): δ 11.05 (s, 1H), 7.2 (m, 3H), 3.78 (s, 3H), 3.6 (br, 1H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07425552B2uspto-grants-2008_09