Réaction #51477

ord-17b4b0c4ef9743189e11324bbc944562

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe reaction was partitioned with 1 N HCl
  2. 2
    AutreThe organic layer was separated
  3. 3
    Lavagewashed with aqueous bicarbonate
  4. 4
    Séchagedried (Na2SO4)
  5. 5
    Autrethe solvent was removed in vacuo

Mode opératoire

To homopiperonylamine hydrochloride (2.14 g, 10.6 mmol) (a compound of formula (Y7)) in CH2Cl2 (20 mL) in an ice bath was added triethylamine (3.1 mL, 21 mmol) and chloroacetyl chloride (0.85 mL, 10 mmol) (a compound of formula (Y6)). After warming to ambient temperature and stirring for 16 hours, the reaction was partitioned with 1 N HCl. The organic layer was separated, washed with aqueous bicarbonate, dried (Na2SO4), and the solvent was removed in vacuo to give 1.8 g of 2-chloro-N-[2-(1,3-benzodioxol-5-yl)ethyl]acetamide, a compound of formula (Y8).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06849739B2uspto-grants-2005_02