Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721692Generated: November 2, 2026

tert-Butyldimethylsilyl chloride → (2S,4R)-4-(tert-butyldimethylsilyloxy)-4-(3-bromophenyl)-2-methyltetrahydropyran

https://huagongshe.com/reaction/1721692

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(2S,4R)-4-hydroxy-4-(3-bromophenyl)-2-methyltetrahydropyranHCID 54527261—
Product(2S,4R)-4-(tert-butyldimethylsilyloxy)-4-(3-bromophenyl)-2-methyltetrahydropyranHCID 5410492278%

Reaction Steps

Using an analogous procedure to that described in the portion of Example 18 which is concerned with the preparation of starting materials, the 4-(3-bromophenyl)-2-methyltetrahydropyran so obtained was reacted with tert-butyldimethylsilyl chloride to give (2S,4R)-4-(tert-butyldimethylsilyloxy)-4-(3-bromophenyl)-2-methyltetrahydropyran in 78% yield as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512594
Source datasetuspto-grants-1996_04
ORD IDord-d33033058b09445aafc21a85caae4cbe
Source noteuspto-grants-1996_04