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2,2-dimethyl-cyclohexanone 2,4,6-tri-isopropyl-benzenesulfonyl hydrazone

Base Information
  • Chemical Name:2,2-dimethyl-cyclohexanone 2,4,6-tri-isopropyl-benzenesulfonyl hydrazone
  • CAS No.:389636-54-8
  • Molecular Formula:C23H38N2O2S
  • Molecular Weight:406.633
  • Hs Code.:
2,2-dimethyl-cyclohexanone 2,4,6-tri-isopropyl-benzenesulfonyl hydrazone

Synonyms:2,2-dimethyl-cyclohexanone 2,4,6-tri-isopropyl-benzenesulfonyl hydrazone

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Chemical Property of 2,2-dimethyl-cyclohexanone 2,4,6-tri-isopropyl-benzenesulfonyl hydrazone
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Technology Process of 2,2-dimethyl-cyclohexanone 2,4,6-tri-isopropyl-benzenesulfonyl hydrazone

There total 1 articles about 2,2-dimethyl-cyclohexanone 2,4,6-tri-isopropyl-benzenesulfonyl hydrazone 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:
2,2-dimethyl-cyclohexanone 2,4,6-tri-isopropyl-benzenesulfonyl hydrazone; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;
With Triisopropyl borate; In tetrahydrofuran; hexane; at 0 ℃; for 1h;
(2E,4E,6Z,8E)-9-Iodo-3,7-dimethyl-nona-2,4,6,8-tetraenoic acid ethyl ester; With TlOH; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; hexane; at 25 ℃; for 1h; Further stages.;
DOI:10.1021/jo010711v
Guidance literature:
Multi-step reaction with 2 steps
1.1: n-BuLi / tetrahydrofuran; hexane / 0.5 h / -78 °C
1.2: B(OPr-i)3 / tetrahydrofuran; hexane / 1 h / 0 °C
1.3: 97 percent / aq. TlOH / Pd(PPh3)4 / tetrahydrofuran; hexane / 1 h / 25 °C
2.1: 92 percent / aq. KOH / ethanol / 0.5 h / Heating
With potassium hydroxide; n-butyllithium; In tetrahydrofuran; ethanol; hexane; 1.1: Shapiro reaction / 1.3: Suzuki coupling;
DOI:10.1021/jo010711v
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