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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490998Generated: October 30, 2026

HCID 49765219, compound → tert-Butyl [(3S,5S)-5-methylpiperidin-3-yl]carbamate

https://huagongshe.com/reaction/490998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 49765219HCID 49765219—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl [(3S,5S)-5-methylpiperidin-3-yl]carbamateHCID 24757764—

Reaction Conditions

Temperature45 °C

Reaction Steps

A 40 L pressure vessel is charged with 0.6 Kg 50% wet, solid palladium on carbon (E101, 10 wt. %) under flow of nitrogen. A solution of 3.2 Kg intermediate (7) in 13.7 Kg of absolute ethanol is then charged to the reactor under nitrogen. The reactor is purged with nitrogen and is then pressurized with hydrogen at 45 psi. The reaction is then heated to 45° C. while maintaining a hydrogen pressure of 45 psi. The reaction is monitored by TLC or LC until complete. The reaction is cooled to ambient temperature, vented, and purged with nitrogen. The reactor contents are filtered through a bed of Celite and the solids are washed with 2.8 Kg of absolute ethanol. The filtrate is concentrated by rotary evaporation under vacuum until a waxy solid is obtained to afford intermediate (8): TLC Rf (Silica F254, 70:30 v/v ethyl acetate-hexanes, KMnO4 stain)=0.12; 1H NMR (300 MHz, CDCl3) δ 5.31 (br s, 1H), 3.80-3.68 (m, 1H), 2.92 (d, J=11.4 Hz, 1H), 2.77 (AB quart, JAB=12.0 Hz, Δv=50.2 Hz, 2H), 2.19 (t, J=10.7 Hz, 1H), 1.82-1.68 (m, 2H), 1.54 (br s, 1H), 1.43 (s, 9H), 1.25-1.15 (m, 1H), 0.83 (d, J=6.6 Hz, 3H); 13C NMR (75 MHz, CDCl3) δ 155.3, 78.9, 54.3, 50.8, 45.3, 37.9, 28.4, 27.1, 19.2; MS (ESI+) m/z 215 (M+H), 429 (2M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528264B2
Source datasetuspto-grants-2009_05
ORD IDord-75c5d98803d740c6a06f83445de6f37e
Source noteuspto-grants-2009_05