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(+/-)-17-phenoxy-18,19,20-trinor-6,7E-epoxy-1E,8E,10E,12Z,15Z-eicosapentaene

Base Information
  • Chemical Name:(+/-)-17-phenoxy-18,19,20-trinor-6,7E-epoxy-1E,8E,10E,12Z,15Z-eicosapentaene
  • CAS No.:109707-57-5
  • Molecular Formula:C23H28O2
  • Molecular Weight:336.474
  • Hs Code.:
(+/-)-17-phenoxy-18,19,20-trinor-6,7E-epoxy-1E,8E,10E,12Z,15Z-eicosapentaene

Synonyms:

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Chemical Property of (+/-)-17-phenoxy-18,19,20-trinor-6,7E-epoxy-1E,8E,10E,12Z,15Z-eicosapentaene
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Technology Process of (+/-)-17-phenoxy-18,19,20-trinor-6,7E-epoxy-1E,8E,10E,12Z,15Z-eicosapentaene

There total 7 articles about (+/-)-17-phenoxy-18,19,20-trinor-6,7E-epoxy-1E,8E,10E,12Z,15Z-eicosapentaene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 5 steps
1: 1.) ethylmagnesium bromide / 1.) THF, cuprous chloride, 65 deg C; 2.) room temp., 3 h
2: 95 percent / carbon tetrabromide, triphenylphosphine / CH2Cl2 / 4 h / 0 °C
3: 70 percent / acetonitrile / 4 h / Heating
4: 1.62 g / H2 / Pd/BaSO4 / ethyl acetate; pyridine
5: 1.) lithium diisopropylamide / 1.) THF, hexane, -78 deg C, 30 min.; 2.) 20 deg C, 24 h
With carbon tetrabromide; ethylmagnesium bromide; hydrogen; triphenylphosphine; lithium diisopropyl amide; Pd-BaSO4; In pyridine; dichloromethane; ethyl acetate; acetonitrile;
Guidance literature:
Multi-step reaction with 7 steps
1: 1.) butyllithium / 1.) THF, -40 deg C, 1.5 h; 2.) 60 deg C, 3 h
2: 70 percent / PBr3, pyridine / diethyl ether / 1.) -30 deg C, 2 h; 2.) 20 deg C, 3 h; 30 deg C, 45 min
3: 1.) ethylmagnesium bromide / 1.) THF, cuprous chloride, 65 deg C; 2.) room temp., 3 h
4: 95 percent / carbon tetrabromide, triphenylphosphine / CH2Cl2 / 4 h / 0 °C
5: 70 percent / acetonitrile / 4 h / Heating
6: 1.62 g / H2 / Pd/BaSO4 / ethyl acetate; pyridine
7: 1.) lithium diisopropylamide / 1.) THF, hexane, -78 deg C, 30 min.; 2.) 20 deg C, 24 h
With pyridine; n-butyllithium; carbon tetrabromide; ethylmagnesium bromide; hydrogen; phosphorus tribromide; triphenylphosphine; lithium diisopropyl amide; Pd-BaSO4; In pyridine; diethyl ether; dichloromethane; ethyl acetate; acetonitrile;
Guidance literature:
Multi-step reaction with 6 steps
1: 70 percent / PBr3, pyridine / diethyl ether / 1.) -30 deg C, 2 h; 2.) 20 deg C, 3 h; 30 deg C, 45 min
2: 1.) ethylmagnesium bromide / 1.) THF, cuprous chloride, 65 deg C; 2.) room temp., 3 h
3: 95 percent / carbon tetrabromide, triphenylphosphine / CH2Cl2 / 4 h / 0 °C
4: 70 percent / acetonitrile / 4 h / Heating
5: 1.62 g / H2 / Pd/BaSO4 / ethyl acetate; pyridine
6: 1.) lithium diisopropylamide / 1.) THF, hexane, -78 deg C, 30 min.; 2.) 20 deg C, 24 h
With pyridine; carbon tetrabromide; ethylmagnesium bromide; hydrogen; phosphorus tribromide; triphenylphosphine; lithium diisopropyl amide; Pd-BaSO4; In pyridine; diethyl ether; dichloromethane; ethyl acetate; acetonitrile;
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