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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051517Generated: November 1, 2026

Methanol → (+/-)-trans-3-Methyl norfentanyl

https://huagongshe.com/reaction/2051517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 14987178HCID 14987178—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product(+/-)-trans-3-Methyl norfentanylHCID 14969498—

Reaction Steps

A mixture of trans-N-benzyloxycarbonyl-3-methyl-4-[(1-oxopropyl)phenylamino]-piperidine (1.5 g, 3.94 mmol), 10% Pd-C (200 mg), methanol (20 ml), and acetic acid (20 ml) is hydrogenated at 50 psi for 24 hours. The resultant suspension is filtered through a bed of Celite and the filtrate concentrated. The residue is diluted with ethyl acetate (50 ml), basified to pH 11 with 2N NaOH and shaken. The organic layer is separated, dried over magnesium sulfate, and concentrated to trans-3-methyl-4-[(1-oxopropyl)-phenylamino]-piperidine: 720 mg; 96%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05019583
Source datasetuspto-grants-1991_05
ORD IDord-da1dd493f8a7464c9f712955394115f3
Source noteuspto-grants-1991_05