HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392022Generated: October 29, 2026
Sodium borohydride → 4-(3-Azidopropoxy)-2,6-dihydroxymethylpyridine
https://huagongshe.com/reaction/392022
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | Diethyl-4-(3-azidopropoxy)-2,6-pyridinedicarboxylate | HCID 22323654 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(3-Azidopropoxy)-2,6-dihydroxymethylpyridine | HCID 54342682 | — |
Reaction Steps
To a stirred solution of Diethyl-4-(3-azidopropoxy)-2,6-pyridinedicarboxylate (4.2 mmol) in dichloromethane (10 mL) and absolute ethanol (15 mL), was added in portions, NaBH4 (4.2 mmol) at 25° C. Powdered CaCl2 (4.2 mmol) was added cautiously in small portions and the evolution of hydrogen was allowed to cease before each further addition. The reaction mixture was stirred for 2 hours. Water (100 mL) was added and the reaction mixture was extracted several times with ethyl acetate. The ethyl acetate layers were combined dried (MgSO4and concentrated in vacuo. The resultant residue was purified by silica gel flash column chromatography to give the title compound. 1H NMR (DMSO) δ 2.00 (m, 2H, CH2), 3.52 (t, 2H, CH2), 4.13 (t, 2H, CH2), 4.45 (d, 4H, 2×CH2), 5.36 (t, 2H, 2×OH), 6.87 (s, 2H, 2×AR
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06800444B1 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-3912e7dd11f3490bbde81b1d4dac940f |
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| Source note | uspto-grants-2004_10 |
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