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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719720Generated: November 1, 2026

HCID 131714328, compound → HCID 131714327, compound

https://huagongshe.com/reaction/1719720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131714328HCID 131714328—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 131714327HCID 131714327—

Reaction Steps

Trans-1-benzyl-3-t-butyldimethylsilyloxy-4-(1-triphenylmethoxyprop-2-yl)piperidine (4.5 g; diastereomer A) was hydrogenated in ethanol (60 cm3) at 60° and 60 p.s.i. pressure over 10% palladium on carbon (0.9 g) for 5 hours. The solution was cooled, filtered through "Avicel" to remove the catalyst and evaporated in vacuo to afford trans-3-t-butyldimethylsilyloxy-4-(1-hydroxyprop-2-yl)piperidine as a crude oil (diastereomer A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04542132
Source datasetuspto-grants-1985_09
ORD IDord-b6b9317ff0c449bb90bb0b0e453db3a6
Source noteuspto-grants-1985_09