Реакция #1283844

ord-5f3a0412159646b3a9627eb862b01ff8

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураunder reflux for 6 hours in a Dean-Stark apparatus
  2. 2
    Температураheated at 60° C. for 3 hours
  3. 3
    ТемператураThe solution was cooled
  4. 4
    Фильтрацияfiltered
  5. 5
    ДругоеThe filtrate was evaporated

Методика

A solution of 3.12 g (0.02 mol) of 3-oxocyclohexanecarboxylate, 1.91 g (0.022 mol) of morpholine and 0.01 g of p-toluenesulfonic acid in 300 ml of toluene was heated under reflux for 6 hours in a Dean-Stark apparatus. The solution was cooled to 0° C. and there were added 2.02 g (0.02 mol) of triethylamine in 5 ml of toluene followed by 3.83 g (0.02 mol) of p-chlorobenzoyl chloride in 30 ml of toluene over a period of 0.5 hour. The mixture was stirred at 20° C. for 3 hours and then heated at 60° C. for 3 hours. The solution was cooled and filtered. The filtrate was evaporated to give ethyl 2-(4-chlorobenzoyl)-1-morpholino-4-cyclohexenecarboxylate as a gum which was dissolved in 10 ml of ethanol and 5 ml of pyridine and treated with 1.4 g (0.02 mol) of hydroxylamine hydrochloride. The mixture was then heated under reflux for 2 hours. The solvents were removed by evaporation, 2N hydrochloric acid was added to the residue and the product was extracted with diethyl ether. Evaporation of the ethereal extract gave 1 g of methyl 3-(4-chlorophenyl)-4,5,6,7-tetrahydro-2,1-benzisoxazole-6-carboxylate of melting point 141°-143° C. (from ethyl acetate/hexane).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05114960uspto-grants-1992_05