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3-((1Z,3E)-5-Bromo-3-methyl-penta-1,3-dienyl)-2,4,4-trimethyl-cyclohex-2-enone

Base Information Edit
  • Chemical Name:3-((1Z,3E)-5-Bromo-3-methyl-penta-1,3-dienyl)-2,4,4-trimethyl-cyclohex-2-enone
  • CAS No.:79749-53-4
  • Molecular Formula:C15H21BrO
  • Molecular Weight:297.235
  • Hs Code.:
  • Mol file:79749-53-4.mol
3-((1Z,3E)-5-Bromo-3-methyl-penta-1,3-dienyl)-2,4,4-trimethyl-cyclohex-2-enone

Synonyms:3-((1Z,3E)-5-Bromo-3-methyl-penta-1,3-dienyl)-2,4,4-trimethyl-cyclohex-2-enone

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Chemical Property of 3-((1Z,3E)-5-Bromo-3-methyl-penta-1,3-dienyl)-2,4,4-trimethyl-cyclohex-2-enone Edit
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Technology Process of 3-((1Z,3E)-5-Bromo-3-methyl-penta-1,3-dienyl)-2,4,4-trimethyl-cyclohex-2-enone

There total 8 articles about 3-((1Z,3E)-5-Bromo-3-methyl-penta-1,3-dienyl)-2,4,4-trimethyl-cyclohex-2-enone 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 4 steps
1: 92 percent / p-toluenesulfonic acid / 1.) 5 deg C, 2.) RT, 10 min
2: 1.) n-BuLi / 1.) ether, hexane, RT, 15 min, 2.) 22 deg C, 1 h
3: 72 percent / H2, potassium carbonate / Lindlar catalyst / toluene / 3 h / 20 °C / 760 Torr
4: PBr3 / diethyl ether / 0.08 h / Ambient temperature
With n-butyllithium; hydrogen; phosphorus tribromide; potassium carbonate; toluene-4-sulfonic acid; Lindlar's catalyst; In diethyl ether; toluene;
DOI:10.1021/jo00132a028
Guidance literature:
Multi-step reaction with 6 steps
1: 1.) LDA / 1.) THF, hexane, -60 deg C, 90 min, 2.) a) 3 min, b) RT, 2 h
2: 85 percent / NaH / methanol / 3 h / Heating
3: 91 percent / p-toluenesulfonic acid / benzene / 3 h / Heating
4: 1.) n-BuLi / 1.) ether, hexane, RT, 15 min, 2.) 22 deg C, 1 h
5: 72 percent / H2, potassium carbonate / Lindlar catalyst / toluene / 3 h / 20 °C / 760 Torr
6: PBr3 / diethyl ether / 0.08 h / Ambient temperature
With n-butyllithium; hydrogen; phosphorus tribromide; sodium hydride; potassium carbonate; toluene-4-sulfonic acid; lithium diisopropyl amide; Lindlar's catalyst; In methanol; diethyl ether; toluene; benzene;
DOI:10.1021/jo00132a028
Guidance literature:
Multi-step reaction with 5 steps
1: 85 percent / NaH / methanol / 3 h / Heating
2: 91 percent / p-toluenesulfonic acid / benzene / 3 h / Heating
3: 1.) n-BuLi / 1.) ether, hexane, RT, 15 min, 2.) 22 deg C, 1 h
4: 72 percent / H2, potassium carbonate / Lindlar catalyst / toluene / 3 h / 20 °C / 760 Torr
5: PBr3 / diethyl ether / 0.08 h / Ambient temperature
With n-butyllithium; hydrogen; phosphorus tribromide; sodium hydride; potassium carbonate; toluene-4-sulfonic acid; Lindlar's catalyst; In methanol; diethyl ether; toluene; benzene;
DOI:10.1021/jo00132a028
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