benzyl ((1S,2R)-2-((tert-butyldimethylsilyl)oxy)-1-(1,3,4-oxadiazol-2-yl)propyl)carbamate

Base Information

Chemical Name:benzyl ((1S,2R)-2-((tert-butyldimethylsilyl)oxy)-1-(1,3,4-oxadiazol-2-yl)propyl)carbamate
CAS No.:1621508-25-5
Molecular Formula:C₁₉H₂₉N₃O₄Si
Molecular Weight:391.542
Hs Code.:

Synonyms:benzyl ((1S,2R)-2-((tert-butyldimethylsilyl)oxy)-1-(1,3,4-oxadiazol-2-yl)propyl)carbamate

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Chemical Property of benzyl ((1S,2R)-2-((tert-butyldimethylsilyl)oxy)-1-(1,3,4-oxadiazol-2-yl)propyl)carbamate

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Technology Process of benzyl ((1S,2R)-2-((tert-butyldimethylsilyl)oxy)-1-(1,3,4-oxadiazol-2-yl)propyl)carbamate

There total 4 articles about benzyl ((1S,2R)-2-((tert-butyldimethylsilyl)oxy)-1-(1,3,4-oxadiazol-2-yl)propyl)carbamate 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: 68.0%

: 1621508-24-4
benzyl ((2S,3R)-3-((tert-butyldimethylsilyl)oxy)-1-hydrazinyl-1-oxobutan-2-yl)carbamate

: 122-51-0
orthoformic acid triethyl ester

: 1621508-25-5
benzyl ((1S,2R)-2-((tert-butyldimethylsilyl)oxy)-1-(1,3,4-oxadiazol-2-yl)propyl)carbamate

Guidance literature:: With toluene-4-sulfonic acid; at 120 ℃; for 3h; Temperature;

Reference yield:

: 57224-63-2
methyl (2S,3R)-2-(benzyloxycarbonylamino)-3-hydroxybutyrate

: 1621508-25-5
benzyl ((1S,2R)-2-((tert-butyldimethylsilyl)oxy)-1-(1,3,4-oxadiazol-2-yl)propyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 12 h / 0 - 20 °C

2: hydrazine hydrate / ethanol / 24 h / 90 °C

3: toluene-4-sulfonic acid / 3 h / 120 °C

With toluene-4-sulfonic acid; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; In ethanol; N,N-dimethyl-formamide;

Reference yield:

: 104410-78-8
(2S,3R)-methyl 2-(((benzyloxy)carbonyl)amino)-3-((tert-butyldimethylsilyl)oxy)butanoate

: 1621508-25-5
benzyl ((1S,2R)-2-((tert-butyldimethylsilyl)oxy)-1-(1,3,4-oxadiazol-2-yl)propyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazine hydrate / ethanol / 24 h / 90 °C

2: toluene-4-sulfonic acid / 3 h / 120 °C

With toluene-4-sulfonic acid; hydrazine hydrate; In ethanol;