HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459512Generated: October 30, 2026
Ammonium Chloride → Ethyl (1S,3R,4R)-3-azido-4-hydroxycyclohexane-1-carboxylate
https://huagongshe.com/reaction/459512
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Ethyl (1S,3S,6R)-7-oxabicyclo[4.1.0]heptane-3-carboxylate | HCID 57416186 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl (1S,3R,4R)-3-azido-4-hydroxycyclohexane-1-carboxylate | HCID 57416187 | 100.3% |
Reaction Steps
Ethyl (1S,3S,4R)-3,4-epoxycyclohexane-1-carboxylate (41 g) was dissolved in N,N-dimethylformamide (300 ml), ammonium chloride (19.3 g) and sodium azide (23.5 g) were successively added at room temperature, and the mixture was then stirred at 75° C. for 13 hours. The reaction mixture was filtered, the filtrate was concentrated to distill off 400 ml of the solvent, the product captured by the filter was put in the residue, and water was added to dissolve the collected product. The solution was extracted with ethyl acetate. The resultant organic layer was washed with water and saturated saline and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain the title compound (51.5 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192968B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-7adf52f01f5c4521a2cf6cbd6dae2f53 |
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| Source note | uspto-grants-2007_03 |
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