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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10526Generated: October 25, 2026

tert-Butyl 4-oxopiperidine-1-carboxylate → 1-Boc-4-(aminomethyl)piperidine

https://huagongshe.com/reaction/10526

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantMethylamine hydrochlorideHCID 6364545—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventMethanolHCID 887—
Product1-Boc-4-(aminomethyl)piperidineHCID 73681793.9%

Reaction Steps

A solution of methylamine hydrochloride (1.01 g, Wako Pure Chemical Industries) and 1-(tert-butoxycarbonyl)-4-oxopiperidine (1.99 g, Aldrich) in methanol (13 ml) was stirred in the presence of platinum oxide (69 mg, Wako Pure Chemical Industries) at room temperature for 3 hours under hydrogen atmosphere of ordinary pressure. The hydrogen was purged with a nitrogen gas, and the platinum catalyst was removed by filtration. Then, the reaction mixture was adjusted to pH of from 10 to 11 with 1 N aqueous sodium hydroxide. The reaction mixture was added with water (10 ml), and the product was extracted three times with ethyl acetate (15 ml for each time). The organic layer was dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:methanol=20:1) to obtain the title compound (2.01 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094789B2
Source datasetuspto-grants-2006_08
ORD IDord-d468fd2f35634bbfb59c0f3c2c17ef5c
Source noteuspto-grants-2006_08