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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870476Generated: November 2, 2026

Piperidin-4-ol → HCID 58072141, compound

https://huagongshe.com/reaction/870476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidin-4-olHCID 79341—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58072141HCID 580721418.2%

Reaction Steps

Into a 250-mL round-bottom flask was placed a solution of piperidin-4-ol (4 g, 39.55 mmol, 1.00 equiv) in tetrahydrofuran (100 mL), TEA (12 g, 118.59 mmol, 3.00 equiv) and tert-butyl(chloro)diphenylsilane (16 g, 58.21 mmol, 1.47 equiv). The resulting solution was stirred for 16 h at room temperature. The solids were filtered out. The filtrate was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:2). Purification afforded 1.1 g (8%) of 4-[(tert-butyldiphenylsilyl)oxy]piperidine as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969557B2
Source datasetuspto-grants-2015_03
ORD IDord-bb0964ffce9f4900a4c4c9e62499dd59
Source noteuspto-grants-2015_03