HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39419Generated: October 26, 2026
Water → trans-(4-Azido-tetrahydro-pyran-3-yl)-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/39419
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Lithium perchlorate | HCID 23665649 | — |
| Reactant | Tert-butyl 3-oxa-7-azabicyclo[4.1.0]heptane-7-carboxylate | HCID 58381262 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | trans-(4-Azido-tetrahydro-pyran-3-yl)-carbamic acid tert-butyl ester | HCID 86656338 | 52.4% |
Reaction Steps
3-Oxa-7-aza-bicyclo[4.1.0]heptane-7-carboxylic acid tert-butyl ester (intermediate E) (5.2 g, 26 mmol) was dissolved in 100 mL acetonitrile. Lithium perchlorate (23 g, 207 mmol) and sodium azide (6.8 g, 104 mmol) were added and the reaction mixture was stirred at 80° C. overnight. 200 mL Water was added. The mixture was extracted three times with diethylether. The combined organic phases were dried on sodium sulfate, filtered and evaporated. Purification of the residue by flash chromatography on silica gel (heptane/ethyl acetate 1:0→1:1) yielded the title compound as a colorless oil (3.3 g, 52%), MS: m/e=186 [(M-butene)+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524909B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-5c9dd2f5be3748d3b48fc749a9973630 |
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| Source note | uspto-grants-2013_09 |
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