(1R,2R)-2-[(tert-butyldiphenylsilyloxy)methyl]-1-(1-ethanoyl)cyclopropane

Base Information

Chemical Name:(1R,2R)-2-[(tert-butyldiphenylsilyloxy)methyl]-1-(1-ethanoyl)cyclopropane
CAS No.:259797-22-3
Molecular Formula:C₂₂H₂₈O₂Si
Molecular Weight:352.549
Hs Code.:

Synonyms:(1R,2R)-2-[(tert-butyldiphenylsilyloxy)methyl]-1-(1-ethanoyl)cyclopropane

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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 (1R,2R)-2-[(tert-butyldiphenylsilyloxy)methyl]-1-(1-ethanoyl)cyclopropane

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Technology Process of (1R,2R)-2-[(tert-butyldiphenylsilyloxy)methyl]-1-(1-ethanoyl)cyclopropane

There total 2 articles about (1R,2R)-2-[(tert-butyldiphenylsilyloxy)methyl]-1-(1-ethanoyl)cyclopropane 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: 89.0%

: 408348-31-2
(1R,2R)-2-(tert-butyldiphenylsilyloxy)methyl-1-formylcyclopropane

: 259797-22-3
(1R,2R)-2-[(tert-butyldiphenylsilyloxy)methyl]-1-(1-ethanoyl)cyclopropane

Guidance literature:: (1R,2R)-2-(tert-butyldiphenylsilyloxy)methyl-1-formylcyclopropane; CH₃MgHal; In tetrahydrofuran; at 20 ℃; for 5h;

With dipyridinium dichromate; 5A molecular sieve; In dichloromethane; at 20 ℃; for 5h;
DOI:10.1021/jo030019v

Reference yield:

: 154001-59-9
(1R,2R)-2-<<(tert-Butyldiphenylsilyl)oxy>methyl>-1-(hydroxymethyl)cyclopropane

: 259797-22-3
(1R,2R)-2-[(tert-butyldiphenylsilyloxy)methyl]-1-(1-ethanoyl)cyclopropane

Guidance literature:: Multi-step reaction with 2 steps

1.1: oxalyl chloride; DMSO; triethylamine / CH₂Cl₂

2.1: tetrahydrofuran / 5 h / 20 °C

2.2: 89 percent / PDC; molecular sieves 5 Angstroem / CH₂Cl₂ / 5 h / 20 °C

With oxalyl dichloride; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; 1.1: Swern oxidation;
DOI:10.1021/jo030019v