Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942490Generated: October 26, 2026

tert-Butyl (6-methylpyridin-3-yl)carbamate → tert-butyl N-(6-methylpiperidin-3-yl)carbamate

https://huagongshe.com/reaction/1942490

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (6-methylpyridin-3-yl)carbamateHCID 23090429—
CatalystAdams' catalystHCID 345198—
SolventAcetic acid ethanolHCID 18476134—
Producttert-butyl N-(6-methylpiperidin-3-yl)carbamateHCID 4260925186.7%

Reaction Steps

To a solution of tert-butyl (6-methylpyridin-3-yl)carbamate (9.00 g) in a mixture of acetic acid-ethanol (1:1, 100 ml) was added platinum (IV) oxide (900 mg), and the mixture was stirred under hydrogen pressure (0.4 MPa) at room temperature for 9 hours. To the mixture was further added platinum (IV) oxide (2.0 g), and the mixture was stirred for 10 hours. The reaction mixture was filtered on celite, and thereto was added toluene. The mixture was concentrated under reduced pressure, and to the residue was added a 5% aqueous potassium carbonates solution. The mixture was extracted with chloroform, and the organic layer was washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated under reduced pressure to give a crude product (8.03 g) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389511B2
Source datasetuspto-grants-2013_03
ORD IDord-e5ebbba9be5f4e7fb438e646c06b1716
Source noteuspto-grants-2013_03