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Se-phenyl 5-ethoxyselenohept-6-enoate

Base Information
  • Chemical Name:Se-phenyl 5-ethoxyselenohept-6-enoate
  • CAS No.:119124-38-8
  • Molecular Formula:C15H20O2Se
  • Molecular Weight:311.283
  • Hs Code.:
Se-phenyl 5-ethoxyselenohept-6-enoate

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Chemical Property of Se-phenyl 5-ethoxyselenohept-6-enoate
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Technology Process of Se-phenyl 5-ethoxyselenohept-6-enoate

There total 6 articles about Se-phenyl 5-ethoxyselenohept-6-enoate 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 6 steps
1: 83 percent / titanium tetrachloride / CH2Cl2 / 0.5 h / -78 °C
2: 55 percent / lithium chloride / dimethylsulfoxide; H2O / 15 h / 150 °C
3: 93 percent / hydrogen / Lindlaar's catalyst poisoned with quinoline / ethanol / 9 h
4: 99 percent / potassium hydroxide / methanol; H2O
5: 1.) sodium hydrogen carbonate, water; 2.) oxalyl chloride / 1.) benzene, 60 deg C; 2.) r.t., 1 h
6: 1.) sodium borohydride / 1.) ethanol, 0 deg C; 2.) ethanol, r.t., 30 h
With potassium hydroxide; sodium tetrahydroborate; oxalyl dichloride; water; hydrogen; titanium tetrachloride; sodium hydrogencarbonate; lithium chloride; Lindlar's catalyst poisoned with quinoline; In methanol; ethanol; dichloromethane; water; dimethyl sulfoxide;
DOI:10.1016/S0040-4020(01)89534-X
Guidance literature:
Multi-step reaction with 5 steps
1: 55 percent / lithium chloride / dimethylsulfoxide; H2O / 15 h / 150 °C
2: 93 percent / hydrogen / Lindlaar's catalyst poisoned with quinoline / ethanol / 9 h
3: 99 percent / potassium hydroxide / methanol; H2O
4: 1.) sodium hydrogen carbonate, water; 2.) oxalyl chloride / 1.) benzene, 60 deg C; 2.) r.t., 1 h
5: 1.) sodium borohydride / 1.) ethanol, 0 deg C; 2.) ethanol, r.t., 30 h
With potassium hydroxide; sodium tetrahydroborate; oxalyl dichloride; water; hydrogen; sodium hydrogencarbonate; lithium chloride; Lindlar's catalyst poisoned with quinoline; In methanol; ethanol; water; dimethyl sulfoxide;
DOI:10.1016/S0040-4020(01)89534-X
Guidance literature:
Multi-step reaction with 4 steps
1: 93 percent / hydrogen / Lindlaar's catalyst poisoned with quinoline / ethanol / 9 h
2: 99 percent / potassium hydroxide / methanol; H2O
3: 1.) sodium hydrogen carbonate, water; 2.) oxalyl chloride / 1.) benzene, 60 deg C; 2.) r.t., 1 h
4: 1.) sodium borohydride / 1.) ethanol, 0 deg C; 2.) ethanol, r.t., 30 h
With potassium hydroxide; sodium tetrahydroborate; oxalyl dichloride; water; hydrogen; sodium hydrogencarbonate; Lindlar's catalyst poisoned with quinoline; In methanol; ethanol; water;
DOI:10.1016/S0040-4020(01)89534-X
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