Reaktion #1737766

ord-75a5fd1c496a480d9f76acda2b8bf924

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with diethyl ether
  2. 2
    WaschenThe extract was washed four times with 25 ml of 3 N hydrochloric acid each time
  3. 3
    Waschenwashed with 25 ml of 2 N sodium carbonate solution and several times with water
  4. 4
    Trocknendried over magnesium sulphate
  5. 5
    Einengenconcentrated

Vorschrift

The crude (S)-4-(6-methyloctyloxy)benzoyl chloride obtained was dissolved in 20 ml of toluene and then added dropwise to a solution of 0.26 g of 4-[2-(trans-4-pentylcyclohexyl)ethyl]phenol in 2 ml of pyridine. The reaction mixture was stirred at room temperature overnight, then poured into ice-water and extracted with diethyl ether. The extract was washed four times with 25 ml of 3 N hydrochloric acid each time, then washed with 25 ml of 2 N sodium carbonate solution and several times with water, dried over magnesium sulphate and concentrated. Chromatography of the residual oil on silica gel with toluene gave 0.2 g of (S)-4-(6-methyloctyloxy)benzoic acid 4-[2-(trans-4-pentylcyclohexyl)ethyl]phenyl ester. The product was recrystallized several times from ethanol until the phase transition temperatures were constant. M.p. (C-S) 58°, transition S-S*C 58.5° C., transition S*C -Ch 93° C., cl.p. (Ch-I) 140° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04925278uspto-grants-1990_05