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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432192Generated: November 1, 2026

Cyclohexanecarboxaldehyde → tert-Butyl 1-(cyclohexylmethyl)piperidin-4-ylcarbamate

https://huagongshe.com/reaction/1432192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanecarboxaldehydeHCID 16275—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
Producttert-Butyl 1-(cyclohexylmethyl)piperidin-4-ylcarbamateHCID 22182394—

Reaction Steps

The title compound was prepared (1.83 g, 83%) from tert-butyl piperidin-4-ylcarbamate (1.50 g, 7.48 mmol) and cyclohexanecarbaldehyde (0.84 g, 7.48 mmol) by following the general procedure described for Preparation 3. 1H NMR (400 MHz, CDCl3) δ 4.80 (bs, 1H), 3.71 (m, 1H), 3.63 (m, 2H), 2.53 (m, 2H), 2.43 (m, 2H), 2.00-1.61 (m, 9H), 1.44 (s, 9H), 1.23 (m, 4H), 0.95 (m, 2H); MS (ESI) m/z: Calculated for C17H33N2O2, 297.25; Observed: 297.1 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612078B2
Source datasetuspto-grants-2009_11
ORD IDord-c5e19046229f46d89a35511865395a29
Source noteuspto-grants-2009_11