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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747015Generated: October 30, 2026

Hydrochloric Acid → (2R,3R,4R,5S)-1-(3-chloropropyl)-2-(hydroxymethyl)piperidine-3,4,5-triol

https://huagongshe.com/reaction/1747015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(2R,3R,4R,5S)-3,4,5-tris(benzyloxy)-2-[(benzyloxy)methyl]-1-(3-chloropropyl)piperidineHCID 118407745—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(2R,3R,4R,5S)-1-(3-chloropropyl)-2-(hydroxymethyl)piperidine-3,4,5-triolHCID 11840774783.5%

Reaction Steps

To a stirred solution of (2R,3R,4R,5S)-3,4,5-tris(benzyloxy)-2-[(benzyloxy)methyl]-1-(3-chloropropyl)piperidine 4 (30 g, 49.98 mmol) in a mixture of ethanol (1.2 lit) and aqueous solution of HCl (1M, 100 mL) was added 10% Pd/C (3 g) and the mixture was degassed for 20 min using nitrogen. The reaction mixture was then stirred under 50 psi hydrogen pressure for 32 h. The reaction mixture was filtrate through celite, washed with ethanol (3×100 mL) and the filtrate was concentrated under reduced pressure to get crude hydrochloride salt of (2R,3R,4R,5S)-1-(3-chloropropyl)-2-(hydroxymethyl)piperidine-3,4,5-triol 5 (10 g, 83%) as black oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150557B1
Source datasetuspto-grants-2015_10
ORD IDord-001b30e611214eb0910a4cbe20956f32
Source noteuspto-grants-2015_10