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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869243Generated: October 30, 2026

Methanol → Carbamic acid, N-(4-amino-1-methylcyclohexyl)-, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/869243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAmmonium formateHCID 2723923—
Reactanttert-Butyl (1-methyl-4-oxocyclohexyl)carbamateHCID 21882608—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
ProductCarbamic acid, N-(4-amino-1-methylcyclohexyl)-, 1,1-dimethylethyl esterHCID 2075483292.8%

Reaction Steps

To a mixture of tert-butyl (1-methyl-4-oxocyclohexyl)carbamate (4.00 g) and methanol (50 mL), ammonium formate (10.2 g) and water (5 mL) were added and stirred for 1 hour until they were completely dissolved. Then, 10% palladium on carbon (2.0 g) was added and stirred at room temperature for 65 hours. After insoluble materials were separated by filtration through celite, the solvent was distilled off, and chloroform was added to the resulting residue, followed by drying over anhydrous magnesium sulfate. The solvent was distilled off to give tert-butyl (4-amino-1-methylcyclohexyl)carbamate (3.73 g) as a colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969336B2
Source datasetuspto-grants-2015_03
ORD IDord-2cbd4b36e7ae45179ab9477a99b5524e
Source noteuspto-grants-2015_03