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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396328Generated: October 29, 2026

1,3-Dibenzyl-4-hydroxypiperidine → 4-Hydroxy-3-benzylpiperidine

https://huagongshe.com/reaction/396328

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dibenzyl-4-hydroxypiperidineHCID 23003713—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
SolventHCID 178418361HCID 178418361—
Product4-Hydroxy-3-benzylpiperidineHCID 23003675—

Reaction Steps

A mixture of 1,3-dibenzyl-4-hydroxypiperidine (1.7 g, 6.0 mmole) and 20% palladium hydroxide (0.3 g) in methanol (20 ml) was stirred in hydrogen atmosphere (1 atm.) for 12 hr at 35° C. Catalyst was filtered off, washed with methanol, filtrate was concentrated to dryness to give 4-hydroxy-3-benzylpiperidine as oil. Yield 1.0 g (91%), C12H17NO, m/z 192 (M+1) PMR (CDCl3): 1.66 (1H, m, H3), 1.94 (1H, m, H5), 2.26 (2H, m, H5, & OH, D2O exchangeable), 2.62 (1H, m, H2), 2.74 (1H, m, H6), 3.02 (1H, m, H2), 3.34 (1H, m, H6), 3.52 (1H, bs, NH, D2O exchangeable), 3.9 (1H, m, H4), 4.74 (2H, m, CH2-Ar), 7.28 (5H, m, ArH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608078B2
Source datasetuspto-grants-2003_08
ORD IDord-fbf4a62d9d524262b8f37191a528f44d
Source noteuspto-grants-2003_08