(2R,6R)-2-(l-phenmenthyloxy)-6-phenyl-4-<(tert-butyldimethylsilyl)-oxy>-2H(5,6)-dihydropyran

Base Information

Chemical Name:(2R,6R)-2-(l-phenmenthyloxy)-6-phenyl-4-<(tert-butyldimethylsilyl)-oxy>-2H(5,6)-dihydropyran
CAS No.:104130-23-6
Molecular Formula:C₃₃H₄₈O₃Si
Molecular Weight:520.828
Hs Code.:

Synonyms:(2R,6R)-2-(l-phenmenthyloxy)-6-phenyl-4-<(tert-butyldimethylsilyl)-oxy>-2H(5,6)-dihydropyran

Suppliers and Price of (2R,6R)-2-(l-phenmenthyloxy)-6-phenyl-4-<(tert-butyldimethylsilyl)-oxy>-2H(5,6)-dihydropyran

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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,6R)-2-(l-phenmenthyloxy)-6-phenyl-4-<(tert-butyldimethylsilyl)-oxy>-2H(5,6)-dihydropyran

Chemical Property:

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MSDS Files:: SDS file from LookChem

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Technology Process of (2R,6R)-2-(l-phenmenthyloxy)-6-phenyl-4-<(tert-butyldimethylsilyl)-oxy>-2H(5,6)-dihydropyran

There total 1 articles about (2R,6R)-2-(l-phenmenthyloxy)-6-phenyl-4-<(tert-butyldimethylsilyl)-oxy>-2H(5,6)-dihydropyran 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:

: 100-52-7
benzaldehyde

: 104130-19-0
tert-Butyl-dimethyl-{(E)-1-methylene-3-[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxy]-allyloxy}-silane

: 104130-23-6
(2R,6R)-2-(l-phenmenthyloxy)-6-phenyl-4-<(tert-butyldimethylsilyl)-oxy>-2H(5,6)-dihydropyran

: 104195-01-9
tert-Butyl-dimethyl-{(2S,6R)-6-[(1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyloxy]-2-phenyl-3,6-dihydro-2H-pyran-4-yloxy}-silane

Guidance literature:: With triethylamine; tris{3-(heptafluoropropylhydroxymethylene)-(+)-camphorato}europium(III); Yield given. Multistep reaction. Yields of byproduct given; 1.) hexane, -10 deg C - -20 deg C, 60 h; 2.) methanol, room temperature;
DOI:10.1021/ja00282a035