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2-Octenoic acid, 8-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3,5-dimethylphenyl]-, ethyl ester, (Z)-

Base Information
  • Chemical Name:2-Octenoic acid, 8-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3,5-dimethylphenyl]-, ethyl ester, (Z)-
  • CAS No.:144180-93-8
  • Molecular Formula:C24H40O3Si
  • Molecular Weight:404.665
  • Hs Code.:
2-Octenoic acid,
8-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3,5-dimethylphenyl]-, ethyl
ester, (Z)-

Synonyms:

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Chemical Property of 2-Octenoic acid, 8-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3,5-dimethylphenyl]-, ethyl ester, (Z)-
Chemical Property:
Purity/Quality:
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Technology Process of 2-Octenoic acid, 8-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3,5-dimethylphenyl]-, ethyl ester, (Z)-

There total 5 articles about 2-Octenoic acid, 8-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-3,5-dimethylphenyl]-, ethyl ester, (Z)- 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: 1.) t-BuLi / 1.) pentane, ether, -78 deg C, 1 h, 2.) THF, -78 deg C, 1 h
2: 99 percent / H2 / 5percent Pd/C / ethanol / 12 h / 760 Torr
3: 1.) DMSO, oxalyl chloride, 2.) Et3N / 1.) CH2Cl2, -50 deg C, 15 min, 2.) CH2Cl2, 0 deg C, 1 h
4: diethyl ether / 8 h / Ambient temperature
With oxalyl dichloride; hydrogen; tert.-butyl lithium; dimethyl sulfoxide; triethylamine; palladium on activated charcoal; In diethyl ether; ethanol;
DOI:10.1021/jo00051a038
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) t-BuLi / 1.) pentane, ether, -78 deg C, 1 h, 2.) THF, -78 deg C, 1 h
2: 99 percent / H2 / 5percent Pd/C / ethanol / 12 h / 760 Torr
3: 1.) DMSO, oxalyl chloride, 2.) Et3N / 1.) CH2Cl2, -50 deg C, 15 min, 2.) CH2Cl2, 0 deg C, 1 h
4: diethyl ether / 8 h / Ambient temperature
With oxalyl dichloride; hydrogen; tert.-butyl lithium; dimethyl sulfoxide; triethylamine; palladium on activated charcoal; In diethyl ether; ethanol;
DOI:10.1021/jo00051a038
Guidance literature:
Multi-step reaction with 3 steps
1: 99 percent / H2 / 5percent Pd/C / ethanol / 12 h / 760 Torr
2: 1.) DMSO, oxalyl chloride, 2.) Et3N / 1.) CH2Cl2, -50 deg C, 15 min, 2.) CH2Cl2, 0 deg C, 1 h
3: diethyl ether / 8 h / Ambient temperature
With oxalyl dichloride; hydrogen; dimethyl sulfoxide; triethylamine; palladium on activated charcoal; In diethyl ether; ethanol;
DOI:10.1021/jo00051a038
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