Réaction #3079

ord-ad0e6003b3be4ab6ac0a6c1f57d6ff26

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureThe mixture was then refluxed for 1 hour
  2. 2
    Autrethe organic phase was separated
  3. 3
    Lavagewashed with 10 mL of water
  4. 4
    Séchagedried over magnesium sulfate
  5. 5
    AutreAfter that, the solvent was evaporated under vacuum

Mode opératoire

To a solution of 2.4 g (11.0 mmoles) of the methyl ester of (+)-8-chloro-6hydroxy-octanoic acid (+)-(VIII) (R=Me) and 0.04 g (0.5 mmoles) of pyridine in 8 ml toluene, 1.6 g (13.5 mmoles) of thionyl chloride in 5 ml of toluene were added slowly. The mixture was then refluxed for 1 hour. After cooling to room temperature, the reaction mixture was added to 20 ml ice water and the organic phase was separated and washed with 10 mL of water and dried over magnesium sulfate. After that, the solvent was evaporated under vacuum. The methyl ester of (-)-6,8-Dichloro-octanoic acid (-)-(III), (R=Me) was obtained in a yield of 2.0 g (81% of the theoretical yield). [α]D20 =-30.0° (c=1, benzene).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05731448uspto-grants-1998_03