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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127173Generated: October 30, 2026

Diethyl Ether → trans-2-Aminocyclohexanecarboxylic acid

https://huagongshe.com/reaction/127173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantChloroformHCID 6212—
ReactantSodium AzideHCID 33557—
Reactant(1R,2R)-(-)-1,2-Cyclohexanedicarboxylic acidHCID 720895—
SolventSulfuric AcidHCID 1118—
Producttrans-2-Aminocyclohexanecarboxylic acidHCID 2724640—

Reaction Steps

Trans-cyclohexane-1,2-dicarboxylic acid (8.105 g; racemic modification) is dissolved in conc. sulfuric acid (25 ml) and chloroform (50 ml) and kept at a temperature of 45° C., to which is added sodium azide (3.6 g) in one hour. After this, the solution is stirred for 90 minutes, added with ice water (25 ml) and is added with ether to remove chloroform. Barium carbonate (90 g) is added to the water layer of the solution to effect the neutralization. Barium sulfate is removed from the solution by filtration and the filtrate is concentrated to dryness to result in needle crystals of rac-trans-2-aminocyclohexanecarboxylic acid (referred to as A) having the following characteristics. When a corresponding rac-cis-compound is used as starting material, there is obtained the corresponding cis-compound i.e. rac-cis-aminocyclohexanecarboxylic acid, referred to as B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04255347
Source datasetuspto-grants-1981_03
ORD IDord-ce530529c0df4fd5b00b5bb28ffac51f
Source noteuspto-grants-1981_03