Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401779Generated: October 31, 2026

(6-Bromohexyloxy)-tert-butyldimethylsilane → HCID 67322787, compound

https://huagongshe.com/reaction/1401779

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Bromohexyloxy)-tert-butyldimethylsilaneHCID 4260352—
ReactantHCID 67166643HCID 67166643—
ProductHCID 67322787HCID 67322787—

Reaction Steps

The preparation was carried out as already described starting from 100 mg (0.26 mmol) of 4-[4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)thiazol-2-yl]piperidine hydrochloride and 92 mg (0.31 mmol) of (6-bromohexyloxy)-tert-butyldimethylsilane. The product was purified by means of flash chromatography on silica gel. The protecting group was cleaved off as already described using an HCl solution in dioxane. The product is in the form of the hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907098B2
Source datasetuspto-grants-2014_12
ORD IDord-74a2796b033e4d2e822dcb9e524ab0f3
Source noteuspto-grants-2014_12