(1S,2S)-1-Phenyl-2-((E)-(S)-1-phenyl-3-trimethylsilanyl-allyl)-propane-1,3-diol

Base Information

Chemical Name:(1S,2S)-1-Phenyl-2-((E)-(S)-1-phenyl-3-trimethylsilanyl-allyl)-propane-1,3-diol
CAS No.:264613-85-6
Molecular Formula:C₂₁H₂₈O₂Si
Molecular Weight:340.538
Hs Code.:

Synonyms:(1S,2S)-1-Phenyl-2-((E)-(S)-1-phenyl-3-trimethylsilanyl-allyl)-propane-1,3-diol

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Chemical Property of (1S,2S)-1-Phenyl-2-((E)-(S)-1-phenyl-3-trimethylsilanyl-allyl)-propane-1,3-diol

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Technology Process of (1S,2S)-1-Phenyl-2-((E)-(S)-1-phenyl-3-trimethylsilanyl-allyl)-propane-1,3-diol

There total 4 articles about (1S,2S)-1-Phenyl-2-((E)-(S)-1-phenyl-3-trimethylsilanyl-allyl)-propane-1,3-diol 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:

Reference yield: 95.0%

: 264613-83-4
methyl (2R,3S)-(E)-2-[(S)-hydroxyphenylmethyl]-3-phenyl-5-trimethylsilyl4-pentenoate

: 264613-85-6
(1S,2S)-1-Phenyl-2-((E)-(S)-1-phenyl-3-trimethylsilanyl-allyl)-propane-1,3-diol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; at 0 - 20 ℃; for 1h;
DOI:10.1021/jo991635n

Reference yield:

: 103-26-4,1754-62-7
Methyl cinnamate

: 264613-85-6
(1S,2S)-1-Phenyl-2-((E)-(S)-1-phenyl-3-trimethylsilanyl-allyl)-propane-1,3-diol

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrahydrofuran / 0.25 h / -78 °C

1.2: 98 percent / tetrahydrofuran / 1 h / -78 - 0 °C

2.1: 94 percent / pyridine / benzene / 1 h / Heating

3.1: 95 percent / LiAlH₄ / diethyl ether / 1 h / 0 - 20 °C

With pyridine; lithium aluminium tetrahydride; In tetrahydrofuran; diethyl ether; benzene; 1.1: Addition / 1.2: Addition / 2.1: Elimination / 3.1: Reduction;
DOI:10.1021/jo991635n

Reference yield:

: p-tolyl α-lithio-β-(trimethylsilyl)ethyl sulfoxide

: 264613-85-6
(1S,2S)-1-Phenyl-2-((E)-(S)-1-phenyl-3-trimethylsilanyl-allyl)-propane-1,3-diol

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrahydrofuran / 0.25 h / -78 °C

1.2: 98 percent / tetrahydrofuran / 1 h / -78 - 0 °C

2.1: 94 percent / pyridine / benzene / 1 h / Heating

3.1: 95 percent / LiAlH₄ / diethyl ether / 1 h / 0 - 20 °C

With pyridine; lithium aluminium tetrahydride; In tetrahydrofuran; diethyl ether; benzene; 1.1: Addition / 1.2: Addition / 2.1: Elimination / 3.1: Reduction;
DOI:10.1021/jo991635n