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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244068Generated: October 25, 2026

1-Aminocyclohexanecarboxylic acid → Methyl 1-aminocyclohexane-1-carboxylate hydrochloride

https://huagongshe.com/reaction/244068

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Aminocyclohexanecarboxylic acidHCID 1366—
ReactantDiethyl EtherHCID 3283—
ReactantThionyl ChlorideHCID 24386—
SolventMethanolHCID 887—
ProductMethyl 1-aminocyclohexane-1-carboxylate hydrochlorideHCID 22645079—

Reaction Steps

To a suspension of 2 g (14 mmol) of 1-aminocyclohexanecarboxylic acid in 20 mL of methanol is sparged hydrogen chloride for 2 minutes. 1.2 mL (16.8 mmol) of thionyl chloride are added to the solution obtained and the reaction medium is refluxed for 6 hours. After cooling, the mixture is concentrated under reduced pressure and the residue obtained is taken up in 5 mL of methanol. 50 mL of ether are added so as to precipitate 2.3 g of methyl 1-aminocyclohexanecarboxylate hydrochloride in the form of a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653276B2
Source datasetuspto-grants-2014_02
ORD IDord-4e12714f91244160b488a881e4366428
Source noteuspto-grants-2014_02