Réaction #1563909

ord-8b74519ed7674fdcb4087268b86d389e

Équation de réaction

CC(=O)Nc1cc2c(cc1I)OCO2
N-(6-iodobenzo[d][1,3]dioxol-5-yl)acetamide
[Na+].[OH-]
NaOH
Nc1cc2c(cc1I)OCO2
6-iodobenzo[d][1,3]dioxol-5-amine
Rendement 98.5%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureto reflux
  2. 2
    TempératureThe mixture was cooled
  3. 3
    Autrethe solvent was removed under vacuum
  4. 4
    AutreThe residue was partitioned between methylene chloride (100 mL) and water (100 mL)
  5. 5
    LavageThe organic layer was washed with water (2×100 mL)
  6. 6
    Séchagedried (MgSO4)
  7. 7
    Autreevaporated under vacuum

Mode opératoire

A solution of N-(6-iodobenzo[d][1,3]dioxol-5-yl)acetamide (200 mg, 0.656 mmol) and NaOH (1.31 g, 32.8 mmol) in ethanol (26 mL) and water (6 mL) was heated to reflux with stirring for 4 h. The mixture was cooled and the solvent was removed under vacuum. The residue was partitioned between methylene chloride (100 mL) and water (100 mL). The organic layer was washed with water (2×100 mL), dried (MgSO4) and evaporated under vacuum to give 6-iodobenzo[d][1,3]dioxol-5-amine (170 mg, 98%) as orange solid. LCMS: 264 [M+1]+; 1H NMR (DMSO-d6) δ 4.88 (s, 2H), 5.87 (s, 2H), 6.47 (s, 1H), 7.07 (s, 1H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09402832B2uspto-grants-2016_08