HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751433Generated: October 27, 2026
Ammonium Chloride → HCID 59754786, compound
https://huagongshe.com/reaction/751433
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Acetic acid, azido-, ethyl ester | HCID 69480 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 5-Methoxy-3-pyridinecarboxaldehyde | HCID 10975549 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59754786 | HCID 59754786 | — |
Reaction Steps
To a cooled (−15° C.) solution of anhydrous EtOH (270 mL) was added sodium metal (4.46 g, 0.194 mol) slowly. After complete reaction a mixture of 3-formyl-5-methoxypyridine (7.5 g, 54.7 mmol) and ethylazidoacetate (25.0 g, 0.194 mol) was added so as to maintain an internal temperature of −15° C. The reaction mixture was kept at −15° C. for 72 hours after which it was poured into a 30% aq. NH4Cl solution, extracted with EtOAc (2×250 mL), the organic phase dried (MgSO4), filtered and evaporated in vacuo. The residue was purified on silica gel eluting with a gradient of 0 to 35% EtOAc in hexanes to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405302B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-4982af0292d140d6a58c0851a44444ba |
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| Source note | uspto-grants-2008_07 |
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