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[2-(1S,2E)-1-(cumyldimethylsiloxy)but-2-enyl](2R)-2,4-dihydroxybutyl acetate

Base Information
  • Chemical Name:[2-(1S,2E)-1-(cumyldimethylsiloxy)but-2-enyl](2R)-2,4-dihydroxybutyl acetate
  • CAS No.:865308-31-2
  • Molecular Formula:C21H34O5Si
  • Molecular Weight:394.583
  • Hs Code.:
[2-(1S,2E)-1-(cumyldimethylsiloxy)but-2-enyl](2R)-2,4-dihydroxybutyl acetate

Synonyms:[2-(1S,2E)-1-(cumyldimethylsiloxy)but-2-enyl](2R)-2,4-dihydroxybutyl acetate

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Chemical Property of [2-(1S,2E)-1-(cumyldimethylsiloxy)but-2-enyl](2R)-2,4-dihydroxybutyl acetate
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Technology Process of [2-(1S,2E)-1-(cumyldimethylsiloxy)but-2-enyl](2R)-2,4-dihydroxybutyl acetate

There total 7 articles about [2-(1S,2E)-1-(cumyldimethylsiloxy)but-2-enyl](2R)-2,4-dihydroxybutyl acetate 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 5 steps
1: 83 percent / pyridine / 0 °C
2: 92 percent / DIBAL / CH2Cl2 / -18 °C
3: 45 percent / lithium di-tert-butylbiphenylide / tetrahydrofuran / -78 °C
4: 98 percent / pyridine; DMAP / 20 °C
5: aq. HCl / tetrahydrofuran / 20 °C
With pyridine; hydrogenchloride; dmap; lithium di-tert-butylbiphenylide; diisobutylaluminium hydride; In tetrahydrofuran; dichloromethane;
DOI:10.1039/b507401k
Guidance literature:
Multi-step reaction with 5 steps
1: 83 percent / pyridine / 0 °C
2: 92 percent / DIBAL / CH2Cl2 / -18 °C
3: 45 percent / lithium di-tert-butylbiphenylide / tetrahydrofuran / -78 °C
4: 98 percent / pyridine; DMAP / 20 °C
5: aq. HCl / tetrahydrofuran / 20 °C
With pyridine; hydrogenchloride; dmap; lithium di-tert-butylbiphenylide; diisobutylaluminium hydride; In tetrahydrofuran; dichloromethane;
DOI:10.1039/b507401k
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