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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225483Generated: November 2, 2026

methyl 4-(N-benzylamino)-1-methyl-1-cyclohexanecarboxylate → Methyl 4-amino-1-methylcyclohexane-1-carboxylate

https://huagongshe.com/reaction/2225483

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 4-(N-benzylamino)-1-methyl-1-cyclohexanecarboxylateHCID 19004646—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductMethyl 4-amino-1-methylcyclohexane-1-carboxylateHCID 1900474768.9%

Reaction Steps

0.2 g of 10% palladium-carbon was added to a solution of 3.1 g of methyl 4-(N-benzylamino)-1-methyl-1-cyclohexanecarboxylate (Example 15) in 200 ml of methanol. The solution was reacted at room temperature under normal-pressure hydrogen gas. The reaction was stopped after 20 hours, the catalyst was filtered out, and the solvent was removed in vacuo from the filtrate. As a result, 1.4 g of methyl 4-amino-1-methyl-1-cyclohexanecarboxylate was obtained as a pale yellow oil, which had the following physiochemical properties:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344845
Source datasetuspto-grants-1994_09
ORD IDord-37c5bdde4edf4dc9b06b67226728faf9
Source noteuspto-grants-1994_09