HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127173Generated: October 30, 2026
Diethyl Ether → trans-2-Aminocyclohexanecarboxylic acid
https://huagongshe.com/reaction/127173
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | (1R,2R)-(-)-1,2-Cyclohexanedicarboxylic acid | HCID 720895 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | trans-2-Aminocyclohexanecarboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04255347 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-ce530529c0df4fd5b00b5bb28ffac51f |
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| Source note | uspto-grants-1981_03 |
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