HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473331Generated: October 31, 2026
Water → 1,1-Dimethylethyl (3S)-3-(azidomethyl)-3-fluoro-1-piperidinecarboxylate
https://huagongshe.com/reaction/473331
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 1,1-dimethylethyl (3S)-3-fluoro-3-({[(trifluoromethyl)sulfonyl]oxy}methyl)-1-piperidinecarboxylate | HCID 86676799 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,1-Dimethylethyl (3S)-3-(azidomethyl)-3-fluoro-1-piperidinecarboxylate | HCID 86676800 | — |
Reaction Steps
1,1-Dimethylethyl (3S)-3-fluoro-3-({[(trifluoromethyl)sulfonyl]oxy}methyl)-1-piperidinecarboxylate (1 wt) is dissolved in N,N,-dimethylformamide (3 vol) at 20° C. and sodium azide (1.1 eq, 0.20 wt) is added. The resulting suspension is stirred at 20-30° C. for 6 h. TBME (5 vol) and water (9 vol) are added. The mixture is stirred for 5 min and the layers are separated. The aqueous phase is extracted with TBME (5 vol) and the TBME phases are combined. The combined organics are washed with water (2×5 vol), filtered and concentrated under reduced pressure to give the title compound as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633319B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-9f196da54148459595974240aa91cdfd |
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| Source note | uspto-grants-2014_01 |
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