HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253574Generated: October 25, 2026
Ammonium Chloride → (2R,3S)-3-(t-Butoxycarbonylamino)-1-azido-4-cyclohexylbutan-2-ol
https://huagongshe.com/reaction/253574
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | erythro-N-Boc-L-cyclohexylalanine epoxide | HCID 9816868 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2R,3S)-3-(t-Butoxycarbonylamino)-1-azido-4-cyclohexylbutan-2-ol | HCID 14179442 | — |
Reaction Steps
tert-Butyl (S)-2-cyclohexyl-1-((S)-oxiran-2-yl)ethylcarbamate (492 mg, 1.82 mmol), sodium azide (600 mg, 9.2 mmol), and ammonium chloride (540 mg, 10 mmol) were dissolved in MeOH (26 mL). The reaction was heated to 70° C. for 15 h. The solution was cooled to rt and quenched with water (80 mL). The solution was extracted with EtOAc (3×). The combined organic layers were washed with brine, dried over MgSO4, and the solvent was removed. The crude (2R,3S)-3-amino-1-azido-4-cyclohexylbutan-2-ol (524 mg) was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872028B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-059767130c084c31a839ee59f8f6d5af |
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| Source note | uspto-grants-2011_01 |
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