Reacción #1563908

ord-1b032f090cc644bfbffa107053f4af14

Ecuación de reacción

ClI
iodine monochloride
CC(=O)Nc1ccc2c(c1)OCO2
N-(benzo[d][1,3]dioxol-5-yl)acetamide
CC(=O)Nc1cc2c(cc1I)OCO2
N-(6-iodobenzo[d][1,3]dioxol-5-yl)acetamide
Rendimiento 22.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadowashed with saturated sodium thiosulfate (2×150 mL) and brine (150 mL)
  2. 2
    SecadoThe methylene chloride solution was dried (MgSO4)
  3. 3
    Otroevaporated
  4. 4
    Otrothe residue was purified by column chromatography on silica gel (CH2Cl2/petroleum at 20/1)

Procedimiento

A 1.0 M solution of iodine monochloride in methylene chloride (72.6 mL) was added dropwise to a solution of N-(benzo[d][1,3]dioxol-5-yl)acetamide (10 g, 55.8 mmol) in methylene chloride (66 mL) and acetic acid (11 mL). The mixture was stirred under nitrogen overnight and then washed with saturated sodium thiosulfate (2×150 mL) and brine (150 mL). The methylene chloride solution was dried (MgSO4) and evaporated, and the residue was purified by column chromatography on silica gel (CH2Cl2/petroleum at 20/1) to obtain N-(6-iodobenzo[d][1,3]dioxol-5-yl)acetamide (3.7 g, 22%) as a white solid. LCMS: 306 [M+1]+; 1H NMR (DMSO-d6) δ 2.00 (s, 3H), 6.06 (s, 2H), 6.95 (s, 1H), 7.37 (s, 1H), 9.34 (s, 1H).

Fuente

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