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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396319Generated: October 29, 2026

1-Benzyl-4-hydroxy-3-isopropylpiperidine → 4-Hydroxy-3-isopropylpiperidine

https://huagongshe.com/reaction/396319

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-hydroxy-3-isopropylpiperidineHCID 23003711—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
SolventHCID 178418361HCID 178418361—
Product4-Hydroxy-3-isopropylpiperidineHCID 23003673—

Reaction Steps

A mixture of 1-benzyl-4-hydroxy-3-isopropylpiperidine (2.9 g, 12.44 mmole) and 20% palladium hydroxide (0.25 g) in methanol (25 ml) was stirred in hydrogen atmosphere (1 atm.) for 24 hr at 30° C. Catalyst was filtered off, washed with methanol, filtrate was concentrated to dryness to give 4-hydroxy-3-isopropylpiperidine as oil. Yield 1.6 g (80%), C8H17NO, m/z 144 (M+1) PMR (CDCl3): 0.9 (6H, m, 2×CH3), 1.1-1.64 (2H, m, CH & H3), 1.66-2.42 (3H, m, H5, & OH, D2O exchangeable), 2.62 (1H, m, H2), 3.02 (2H, m, H6), 3.45 (1H, bs, NH, D2O exchangeable), 3.54 (1H, m, H6), 4.18 (1H, m, H4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608078B2
Source datasetuspto-grants-2003_08
ORD IDord-d71304b05bb34ec88cf5bcdf5425136a
Source noteuspto-grants-2003_08