benzoic acid (2'R,3'S)-3'-(tert-butyldimethylsilyloxy)tetrahydropyran-2'-ylmethyl ester

Base Information

Chemical Name:benzoic acid (2'R,3'S)-3'-(tert-butyldimethylsilyloxy)tetrahydropyran-2'-ylmethyl ester
CAS No.:234111-57-0
Molecular Formula:C₁₉H₃₀O₄Si
Molecular Weight:350.53
Hs Code.:

Synonyms:benzoic acid (2'R,3'S)-3'-(tert-butyldimethylsilyloxy)tetrahydropyran-2'-ylmethyl ester

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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 benzoic acid (2'R,3'S)-3'-(tert-butyldimethylsilyloxy)tetrahydropyran-2'-ylmethyl ester

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Technology Process of benzoic acid (2'R,3'S)-3'-(tert-butyldimethylsilyloxy)tetrahydropyran-2'-ylmethyl ester

There total 2 articles about benzoic acid (2'R,3'S)-3'-(tert-butyldimethylsilyloxy)tetrahydropyran-2'-ylmethyl ester 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: 97.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 234111-56-9
benzoic acid (2'R,3'S)-3'-hydroxytetrahydropyran-2'-ylmethyl ester

: 234111-57-0
benzoic acid (2'R,3'S)-3'-(tert-butyldimethylsilyloxy)tetrahydropyran-2'-ylmethyl ester

Guidance literature:: With 1H-imidazole; dmap; In dichloromethane; for 4h; Ambient temperature;
DOI:10.1021/jo9901438

Reference yield:

: 51450-45-4
(2R,3S)-2-hydroxymethyltetrahydropyran-3-ol

: 234111-57-0
benzoic acid (2'R,3'S)-3'-(tert-butyldimethylsilyloxy)tetrahydropyran-2'-ylmethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / DMAP / CH₂Cl₂ / 4 h / Ambient temperature

2: 97 percent / imidazole, DMAP / CH₂Cl₂ / 4 h / Ambient temperature

With 1H-imidazole; dmap; In dichloromethane;
DOI:10.1021/jo9901438