Reaktion #2130080

ord-a58eb456274a4d1f8598ce3fcec099bd

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGstirred until the red color
  2. 2
    ExtraktionIt was then extracted with CH2Cl2
  3. 3
    Waschenthe organic layer was washed with water and brine
  4. 4
    Sonstigedried
  5. 5
    Einengenconcentrated
  6. 6
    Sonstigeto get the crude product which
  7. 7
    Sonstigewas purified by column chromatography (mobile phase: petroleum/methylene chloride=1/19)

Vorschrift

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).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08586605B2uspto-grants-2013_11