Reacción #1563911

ord-54e0e932bf944f45b227edc2ba7266aa

Ecuación de reacción

O=S([O-])([O-])=S.[Na+].[Na+]
Na2S2O3
CC(=O)NCc1ccc2c(c1)OCO2
N-(benzo[d][1,3]dioxol-5-ylmethyl)acetamide
ClI
iodine monochloride
CC(=O)NCc1cc2c(cc1I)OCO2
N-((6-iodobenzo[d][1,3]dioxol-5-yl)methyl)acetamide
Rendimiento 38.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGstirred until the red color
  2. 2
    ExtracciónIt was then extracted with CH2Cl2
  3. 3
    Lavadothe organic layer was washed with water and brine
  4. 4
    Otrodried
  5. 5
    Concentraciónconcentrated
  6. 6
    Otroto get the crude product which
  7. 7
    Otrowas purified by column chromatography (mobile phase: petroleum/methylene chloride=1/19)

Procedimiento

N-(benzo[d][1,3]dioxol-5-ylmethyl)acetamide (9.24 g, 47.9 mmol) was added to 1.0 M solution of iodine monochloride in methylene chloride (80 mL). The mixture was stirred at room temperature for 2 hours, and then the mixture was poured into 10% Na2S2O3 and stirred until the red color faded. It was then extracted with CH2Cl2 and the organic layer was washed with water and brine, dried and concentrated to get the crude product which was purified by column chromatography (mobile phase: petroleum/methylene chloride=1/19) to give N-((6-iodobenzo[d][1,3]dioxol-5-yl)methyl)acetamide compound as a white solid (5.82 g, 38%). LC-MS: 320 [M+1]+. 1H-NMR (DMSO-d6): δ 1.89 (s, 3H), 4.11 (d, 2H, J=6.0 Hz), 6.04 (s, 2H), 7.07 (s, 1H), 7.37 (s, 1H), 8.28 (t, 1H, J=6.0 Hz).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09402832B2uspto-grants-2016_08