Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378932Generated: November 3, 2026

N-(2-nitrophenethyl)-1-benzylpiperidin-4-amine → N-(2-aminophenethyl)-1-benzylpiperidin-4-amine

https://huagongshe.com/reaction/2378932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-nitrophenethyl)-1-benzylpiperidin-4-amineHCID 16202487—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventMethanolHCID 887—
ProductN-(2-aminophenethyl)-1-benzylpiperidin-4-amineHCID 21102095—

Reaction Steps

N-(2-Nitrophenethyl)-1-benzylpiperidin-4-amine (1.98 g, 5.83 mmol) was dissolved in methanol (60 mL). Platinum(IV) oxide (55 mg, 0.242 mmol) was added to the mixture. Reaction vessel was placed on a Parr apparatus and charged with 50 psi of hydrogen gas. Reaction shook at room temperature for 75 minutes. Mixture was removed from the apparatus and then filtered over celite. Filtrate was concentrated to dryness. Title compound was obtained as brown oil in quantitative yield. MS (M+H)+=310.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470680B2
Source datasetuspto-grants-2008_12
ORD IDord-e6f0b6eed8fb466199e73cbcb048c494
Source noteuspto-grants-2008_12