4-benzyloxy-(R)-2-((R)-2-tert-butyl-(R)-5-oxo-[1,3]dioxolan-4-yl)butyric acid

Base Information

Chemical Name:4-benzyloxy-(R)-2-((R)-2-tert-butyl-(R)-5-oxo-[1,3]dioxolan-4-yl)butyric acid
CAS No.:1073132-15-6
Molecular Formula:C₁₈H₂₄O₆
Molecular Weight:336.385
Hs Code.:

Synonyms:4-benzyloxy-(R)-2-((R)-2-tert-butyl-(R)-5-oxo-[1,3]dioxolan-4-yl)butyric acid

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-benzyloxy-(R)-2-((R)-2-tert-butyl-(R)-5-oxo-[1,3]dioxolan-4-yl)butyric acid

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Technology Process of 4-benzyloxy-(R)-2-((R)-2-tert-butyl-(R)-5-oxo-[1,3]dioxolan-4-yl)butyric acid

There total 1 articles about 4-benzyloxy-(R)-2-((R)-2-tert-butyl-(R)-5-oxo-[1,3]dioxolan-4-yl)butyric acid 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: 80.0%

: 1073132-19-0
2-((R)-2-benzyloxyethyl)-(R)-3-hydroxysuccinic acid

: 630-19-3
pivalaldehyde

: 1073132-15-6
4-benzyloxy-(R)-2-((R)-2-tert-butyl-(R)-5-oxo-[1,3]dioxolan-4-yl)butyric acid

Guidance literature:: With toluene-4-sulfonic acid; In tetrahydrofuran; hexane; for 5h; Reflux;
DOI:10.1021/jo801708q

Reference yield: 73.0%

: 5292-43-3
bromoacetic acid tert-butyl ester

: 1073132-15-6
4-benzyloxy-(R)-2-((R)-2-tert-butyl-(R)-5-oxo-[1,3]dioxolan-4-yl)butyric acid

: 1073132-14-5
4-benzyloxy-(R)-2-(4-tert-butoxycarbonylmethyl-2-(R)-tert-butyl-(R)-5-oxo-[1,3]dioxolan-4-yl)butyric acid

Guidance literature:: 4-benzyloxy-(R)-2-((R)-2-tert-butyl-(R)-5-oxo-[1,3]dioxolan-4-yl)butyric acid; With lithium hexamethyldisilazane; In tetrahydrofuran; N,N-dimethyl-formamide; at -70 ℃; for 0.833333h;

bromoacetic acid tert-butyl ester; In tetrahydrofuran; N,N-dimethyl-formamide; at -70 ℃; for 0.25h; diastereoselective reaction;
DOI:10.1021/jo801708q