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trifluoro-methanesulfonic acid 3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-cyclohexa-1,5-dienyl ester

Base Information
  • Chemical Name:trifluoro-methanesulfonic acid 3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-cyclohexa-1,5-dienyl ester
  • CAS No.:943448-08-6
  • Molecular Formula:C15H25F3O4SSi
  • Molecular Weight:386.508
  • Hs Code.:
trifluoro-methanesulfonic acid 3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-cyclohexa-1,5-dienyl ester

Synonyms:trifluoro-methanesulfonic acid 3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-cyclohexa-1,5-dienyl ester

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Chemical Property of trifluoro-methanesulfonic acid 3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-cyclohexa-1,5-dienyl ester
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Technology Process of trifluoro-methanesulfonic acid 3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-cyclohexa-1,5-dienyl ester

There total 3 articles about trifluoro-methanesulfonic acid 3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-cyclohexa-1,5-dienyl ester 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:
5-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-cyclohex-2-en-1-one; With lithium diisopropyl amide; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;
N,N-phenylbistrifluoromethane-sulfonimide; In tetrahydrofuran; hexane; at 0 ℃; for 2h; Further stages.;
DOI:10.1021/ol070397c
Guidance literature:
Multi-step reaction with 2 steps
1.1: 13.1 g / diallyl carbonate / Pd2(dba)3 / acetonitrile / 12 h / 20 °C
2.1: LDA / tetrahydrofuran; hexane / 0.5 h / -78 °C
2.2: 79 percent / tetrahydrofuran; hexane / 2 h / 0 °C
With diallylcarbonate; lithium diisopropyl amide; tris(dibenzylideneacetone)dipalladium (0); In tetrahydrofuran; hexane; acetonitrile;
DOI:10.1021/ol070397c
Guidance literature:
Multi-step reaction with 3 steps
1.1: 2,2,6,6-tetramethylpiperidine; n-BuLi / tetrahydrofuran; hexane / -78 - 0 °C
2.1: 13.1 g / diallyl carbonate / Pd2(dba)3 / acetonitrile / 12 h / 20 °C
3.1: LDA / tetrahydrofuran; hexane / 0.5 h / -78 °C
3.2: 79 percent / tetrahydrofuran; hexane / 2 h / 0 °C
With 2,2,6,6-tetramethyl-piperidine; n-butyllithium; diallylcarbonate; lithium diisopropyl amide; tris(dibenzylideneacetone)dipalladium (0); In tetrahydrofuran; hexane; acetonitrile;
DOI:10.1021/ol070397c
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