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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303397Generated: October 30, 2026

HCID 59904582, compound → HCID 59904579, compound

https://huagongshe.com/reaction/2303397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59904582HCID 59904582—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 59904579HCID 59904579110.6%

Reaction Steps

(3S,4S)-4-Benzyl-3,4-dihydroxy-piperidine-1-carboxylic acid benzyl ester 8.2 g (24 mmol) was dissolved in 250 ml EtOH and hydrogenated in the presence of 1.1 g Pd/C, (10%)under atmospheric pressure at r.t. After 16 hours the reaction was complete and the catalyst was filtered off and the solvent was removed under reduced pressure to give 5.5 g (quant., ˜95% purity) (3S,4S)-4-Benzyl-3,4-dihydroxy-piperidine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432985B1
Source datasetuspto-grants-2002_08
ORD IDord-4cd31c308b654abfa9cbc8fb90402c58
Source noteuspto-grants-2002_08