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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409543Generated: November 2, 2026

1-Aminocyclohexanecarboxylic acid → Methyl 1-aminocyclohexanoate

https://huagongshe.com/reaction/1409543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Aminocyclohexanecarboxylic acidHCID 1366—
ReactantTrimethylsilyldiazomethaneHCID 167693—
SolventTetrahydrofurfuryl alcoholHCID 7360—
ProductMethyl 1-aminocyclohexanoateHCID 404881952%

Reaction Steps

To a solution of 1-aminocyclohexanecarboxylic acid (600 mg) in tetrahydrofuran-methanol was added dropwise trimethylsilyl diazomethane (4.2 mL) under ice-cooling and stirring, and the mixture was stirred overnight. The reaction mixture was concentrated in vacuo, and to the residue were added successively diethylether-hexane (1/1) and a solution of 4N hydrochloric acid in ethyl acetate (1.05 mL). The precipitates were collected by filtration and dried to give methyl 1-amino-cyclohexanecarboxylate (423 mg, yield: 52%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921380B2
Source datasetuspto-grants-2014_12
ORD IDord-dac9481abc714010ba21cf2f5cbac49c
Source noteuspto-grants-2014_12