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

Base Information

Chemical Name:(1R,2R)-2-[(tert-butyldiphenylsilyloxy)methyl]-1-[(S)-1-hydroxyethyl]cyclopropane
CAS No.:534584-81-1
Molecular Formula:C₂₂H₃₀O₂Si
Molecular Weight:354.565
Hs Code.:

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

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

There total 10 articles about (1R,2R)-2-[(tert-butyldiphenylsilyloxy)methyl]-1-[(S)-1-hydroxyethyl]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: 88.0%

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

: 534584-81-1
(1R,2R)-2-[(tert-butyldiphenylsilyloxy)methyl]-1-[(S)-1-hydroxyethyl]cyclopropane

Guidance literature:: With potassium trisiamylborohydride; In tetrahydrofuran; dichloromethane; at -78 ℃; for 8h;
DOI:10.1021/jo030019v

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 534585-45-0
(1R,2R)-2-benzyloxymethyl-1-ethanoylcyclopropane

: 534584-81-1
(1R,2R)-2-[(tert-butyldiphenylsilyloxy)methyl]-1-[(S)-1-hydroxyethyl]cyclopropane

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

Guidance literature:: (1R,2R)-2-benzyloxymethyl-1-ethanoylcyclopropane; With potassium trisiamylborohydride; In tetrahydrofuran; dichloromethane; at -78 ℃; for 5h;

With hydrogen; palladium on activated charcoal; In methanol;

tert-butylchlorodiphenylsilane; With 1H-imidazole; In N,N-dimethyl-formamide; Title compound not separated from byproducts;
DOI:10.1021/jo030019v

Reference yield:

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

: 534584-81-1
(1R,2R)-2-[(tert-butyldiphenylsilyloxy)methyl]-1-[(S)-1-hydroxyethyl]cyclopropane

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

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; dichloromethane; at -78 ℃; for 5h; Title compound not separated from byproducts;
DOI:10.1021/jo030019v