{[(2R,3S)-1-(benzyloxy)-2-methylhex-5-en-3-yl]oxy}(tert-butyl)diphenylsilane

Base Information

Chemical Name:{[(2R,3S)-1-(benzyloxy)-2-methylhex-5-en-3-yl]oxy}(tert-butyl)diphenylsilane
CAS No.:1092368-83-6
Molecular Formula:C₃₀H₃₈O₂Si
Molecular Weight:458.716
Hs Code.:

Synonyms:{[(2R,3S)-1-(benzyloxy)-2-methylhex-5-en-3-yl]oxy}(tert-butyl)diphenylsilane

Suppliers and Price of {[(2R,3S)-1-(benzyloxy)-2-methylhex-5-en-3-yl]oxy}(tert-butyl)diphenylsilane

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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 {[(2R,3S)-1-(benzyloxy)-2-methylhex-5-en-3-yl]oxy}(tert-butyl)diphenylsilane

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Technology Process of {[(2R,3S)-1-(benzyloxy)-2-methylhex-5-en-3-yl]oxy}(tert-butyl)diphenylsilane

There total 1 articles about {[(2R,3S)-1-(benzyloxy)-2-methylhex-5-en-3-yl]oxy}(tert-butyl)diphenylsilane 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: 95.0%

: 94233-74-6
(2R,3S)-1-(benzyloxy)-2-methylhex-5-en-3-ol

: 58479-61-1
tert-butylchlorodiphenylsilane

: 1092368-83-6
{[(2R,3S)-1-(benzyloxy)-2-methylhex-5-en-3-yl]oxy}(tert-butyl)diphenylsilane

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 20 ℃; for 10h;
DOI:10.1055/s-2008-1078170

Reference yield: 89.6%

: 1092368-83-6
{[(2R,3S)-1-(benzyloxy)-2-methylhex-5-en-3-yl]oxy}(tert-butyl)diphenylsilane

: 1092368-84-7
5-O-benzyl-3-O-[tert-butyl(diphenyl)silyl]-2,4-dideoxy-4-methyl-D-erythro-pentose

Guidance literature:: With 2,6-dimethylpyridine; sodium periodate; osmium(VIII) oxide; In 1,4-dioxane; water; tert-butyl alcohol; at 25 ℃; for 5h; Inert atmosphere;
DOI:10.1055/s-0029-1216903