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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944858Generated: November 3, 2026

1-Benzyl-4-((6-((tert-butyldimethylsilyl)oxy)hexyl)oxy)piperidine → HCID 58505168, compound

https://huagongshe.com/reaction/1944858

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-((6-((tert-butyldimethylsilyl)oxy)hexyl)oxy)piperidineHCID 57516930—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 58505168HCID 5850516898.3%

Reaction Steps

Intermediate 22 (157 mg, 0.387 mmol) was dissolved in MeOH (5 mL) then added 10% (w/w) Pd/C (41 mg, 0.0387 mmol). The reaction vessel was attached to 3-way valve with balloon containing hydrogen gas. The vessel was evacuated 3 times then back flushed with hydrogen. The resulting suspension was stirred overnight, filtered, and concentrated to give the title compound (120 mg) as clear oil. The compound was used with no further purification. ES/MS calcd for C17H38NO2Si+ 316.3. Found m/z=316.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394829B2
Source datasetuspto-grants-2013_03
ORD IDord-3fbf310c0dfe43c58cab7d547eaeb997
Source noteuspto-grants-2013_03