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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303395Generated: October 31, 2026

HCID 59904582, compound → HCID 59904579, compound

https://huagongshe.com/reaction/2303395

Reaction equation

Participants

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

Reaction Steps

(3R,4R) and (3S,4S)-4-Benzyl-3,4-dihydroxy-piperidine-1-carboxylic acid benzyl ester 1.46 g (4.3 mmol) was dissolved in 30 ml EtOH and hydrogenated in the presence of 400 mg Pd/C (10%) under atmospheric pressure of H2 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 796 mg (3.8 mmol, 89%) (3R,4R) and (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-f5e79b2c44b94b08ad31b0aeaed7f8f5
Source noteuspto-grants-2002_08