(1S,2R,3S)-1-[4-(tert-Butyl-diphenyl-silanyloxymethyl)-phenyl]-4,4,4-trifluoro-2-hydroxymethyl-butane-1,3-diol

Base Information

Chemical Name:(1S,2R,3S)-1-[4-(tert-Butyl-diphenyl-silanyloxymethyl)-phenyl]-4,4,4-trifluoro-2-hydroxymethyl-butane-1,3-diol
CAS No.:211857-39-5
Molecular Formula:C₂₈H₃₃F₃O₄Si
Molecular Weight:518.648
Hs Code.:

Synonyms:(1S,2R,3S)-1-[4-(tert-Butyl-diphenyl-silanyloxymethyl)-phenyl]-4,4,4-trifluoro-2-hydroxymethyl-butane-1,3-diol

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Chemical Property of (1S,2R,3S)-1-[4-(tert-Butyl-diphenyl-silanyloxymethyl)-phenyl]-4,4,4-trifluoro-2-hydroxymethyl-butane-1,3-diol

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Technology Process of (1S,2R,3S)-1-[4-(tert-Butyl-diphenyl-silanyloxymethyl)-phenyl]-4,4,4-trifluoro-2-hydroxymethyl-butane-1,3-diol

There total 1 articles about (1S,2R,3S)-1-[4-(tert-Butyl-diphenyl-silanyloxymethyl)-phenyl]-4,4,4-trifluoro-2-hydroxymethyl-butane-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: 87.0%

: 211857-38-4
Acetic acid (S)-[4-(tert-butyl-diphenyl-silanyloxymethyl)-phenyl]-((2R,5R,6S)-2-tert-butyl-4-oxo-6-trifluoromethyl-[1,3]dioxan-5-yl)-methyl ester

: 211857-39-5
(1S,2R,3S)-1-[4-(tert-Butyl-diphenyl-silanyloxymethyl)-phenyl]-4,4,4-trifluoro-2-hydroxymethyl-butane-1,3-diol

Guidance literature:: With sodium tetrahydroborate; In tetrahydrofuran; methanol; for 7h; Ambient temperature;
DOI:10.1002/hlca.19980810515

Reference yield:

: 211857-39-5
(1S,2R,3S)-1-[4-(tert-Butyl-diphenyl-silanyloxymethyl)-phenyl]-4,4,4-trifluoro-2-hydroxymethyl-butane-1,3-diol

: 211857-44-2
[4-((1S,2R,3S)-1,3-Bis-allyloxy-2-allyloxymethyl-4,4,4-trifluoro-butyl)-phenyl]-methanol

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) NaH / 1.) THF, r.t., 30 min; 2.) THF, reflux, 4 h

2: 87 percent / TBAF / tetrahydrofuran / 3.5 h / Ambient temperature

With tetrabutyl ammonium fluoride; sodium hydride; In tetrahydrofuran;
DOI:10.1002/hlca.19980810515

Reference yield:

: 211857-39-5
(1S,2R,3S)-1-[4-(tert-Butyl-diphenyl-silanyloxymethyl)-phenyl]-4,4,4-trifluoro-2-hydroxymethyl-butane-1,3-diol

: 211857-45-3
1-((1S,2R,3S)-1,3-Bis-allyloxy-2-allyloxymethyl-4,4,4-trifluoro-butyl)-4-bromomethyl-benzene

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) NaH / 1.) THF, r.t., 30 min; 2.) THF, reflux, 4 h

2: 87 percent / TBAF / tetrahydrofuran / 3.5 h / Ambient temperature

3: 90 percent / Ph₃P, CBr₄ / tetrahydrofuran / 16 h / Ambient temperature

With carbon tetrabromide; tetrabutyl ammonium fluoride; sodium hydride; triphenylphosphine; In tetrahydrofuran;
DOI:10.1002/hlca.19980810515