HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486797Generated: October 30, 2026
Dimethylformamide → HCID 118007383, compound
https://huagongshe.com/reaction/1486797
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 118006534 | HCID 118006534 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 118007383 | HCID 118007383 | — |
Reaction Steps
To a stirred solution of (3S,5R)-tert-butyl 3-methyl-5-((tosyloxy)methyl)piperidine-1-carboxylate (0.860 g, 2.232 mmol) in DMF (7 mL) at rt was added sodium azide (0.218 g, 3.347 mmol) after which time the reaction was warmed to 80° C. and stirred an additional 3 h. The completed reaction was cooled to rt, diluted with EtOAc (25 mL) and washed three times with water (5 mL each). The resultant organic layer was dried over anhydrous Na2SO4, filtered, concentrated after which time the crude product was purified over silica gel (Biotage eluting with 0 to 15% EtOAc in heptane gradient) to provide (2R,6R)-tert-butyl 2-(azidomethyl)-6-methylmorpholine-4-carboxylate, 37 (0.545 g, 2.126 mmol, 95.3% yield) as a colorless crystalline solid after concentration of the desired combined fractions and drying in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428495B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-3b63e05f44854546912f43e3d6ff9d7b |
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| Source note | uspto-grants-2016_08 |
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