Reaktion #4378

ord-376b3b80298747838d4894a89b3c46a4

Reaktionsgleichung

ClCCl
methylene chloride
O=C(Cl)C(=O)Cl
oxalyl chloride
COc1ccc(I)c(CC(=O)O)c1
2-iodo-5-methoxybenzeneacetic acid
CNC
dimethylamine
COc1ccc(I)c(CC(=O)N(C)C)c1
N,N-dimethyl-2-iodo-5-methoxybenzeneacetamide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe solution was cooled to 0° C.
  2. 2
    Temperaturto warm to room temperature
  3. 3
    workup.STIRRINGstir for three hours
  4. 4
    WaschenThe organic layer was washed with water, dilute hydrochloric acid, and sodium hydroxide
  5. 5
    TrocknenThe organic layer was dried with MgSO4
  6. 6
    Sonstigeevaporated in vacuo

Vorschrift

A 16.7 g (0.19 mole) sample of oxalyl chloride was added dropwise at 0° C. to a solution of 50.0 g (0.17 mole) of 2-iodo-5-methoxybenzeneacetic acid in 310 ml dry toluene and 31.7 ml of DMF. The mixture was allowed to warm to room temperature and stir for 16 hours. The solution was cooled to 0° C. and dimethylamine gas was admitted until the mixture was strongly basic. The mixture was allowed to warm to room temperature and stir for three hours and methylene chloride was added. The organic layer was washed with water, dilute hydrochloric acid, and sodium hydroxide. The organic layer was dried with MgSO4 and evaporated in vacuo to give 54.2 g of N,N-dimethyl-2-iodo-5-methoxybenzeneacetamide, mp 86°-89° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04725602uspto-grants-1988_02