HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360997Generated: October 31, 2026
Water → Ethyl (1S,3R,4S)-4-azido-3-[(tert-butoxycarbonyl)amino]cyclohexane-1-carboxylate
https://huagongshe.com/reaction/2360997
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Ethyl (1S,3R,4R)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-[(methylsulfonyl)oxy]cyclohexanecarboxylate | HCID 86593060 | — |
| Catalyst | Trioctylmethylammonium chloride | HCID 21218 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Ethyl (1S,3R,4S)-4-azido-3-[(tert-butoxycarbonyl)amino]cyclohexane-1-carboxylate | HCID 57416168 | — |
Reaction Steps
Sodium azide (357.6 mg) and trioctylmethylammonium chloride (335.5 mg) were added at room temperature to a solution (2 mL) of ethyl (1S,3R,4R)-3-[(t-butoxycarbonyl)amino]-4-methanesulfonyloxycyclohexanecarboxylate (1.01 g) in N-methyl-2-pyrrolidone, followed by stirring at 60° C. for 74 hours. Water and ethyl acetate were added to the reaction mixture, and the organic layer was washed with aqueous saturated sodium bicarbonate solution and water, followed by drying over magnesium sulfate anhydrate. The solvent was evaporated under reduced pressure, and the residue was subjected to silica gel column chromatography (n-hexane ethyl acetate=4:1), to thereby yield 706.2 mg of the title compound. Spectral data of this compound were found to be identical with those of the compound of Example 5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686189B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-86758e50913e4a108833f472f8634521 |
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| Source note | uspto-grants-2014_04 |
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