반응 #64016

ord-e0c0568465984b42829b79ad0df936eb

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타is removed under reduced pressure
  2. 2
    기타The residual dark solid is collected
  3. 3
    세척washed sequentially with acetonitrile and ether
  4. 4
    기타Crystallization from ethyl acetate
  5. 5
    기타gave 9.0 g (14%) of isomer A (3: R=4-Cl, n=15), melting at 100°-102° C.

실험 절차

A solution of 32.8 g (0.131 mol) of 1-(4-chlorophenyl)-N-methyl-2-(1H-1,2,4-triazol-1-yl)ethanimine N-oxide (1: R=4-Cl) [prepared by reacting 2-(1H-1,2,4-triazol-1-yl)-4'-chloroacetophenone (35.38 g, 0.160 mol) with N-methylhydroxylamine hydrochloride (20.0 g, 0.240 mol) and NaHCO3 (20.12 g, 0.240 mol) in 500 ml ethanol] and 62.8 ml (0.196 mol) of 1-octadecene (2: n=15) in 400 ml toluene is refluxed for 48 hours under a nitrogen atmosphere. Upon cooling to room temperature the solvent is removed under reduced pressure. The residual dark solid is collected and washed sequentially with acetonitrile and ether. Crystallization from ethyl acetate gave 9.0 g (14%) of isomer A (3: R=4-Cl, n=15), melting at 100°-102° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04767866uspto-grants-1988_08