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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411862Generated: October 29, 2026

Sodium borohydride → 4-(3-Azidopropoxy)-2,6-dihydroxymethylpyridine

https://huagongshe.com/reaction/411862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantCalcium ChlorideHCID 5284359—
ReactantDiethyl-4-(3-azidopropoxy)-2,6-pyridinedicarboxylateHCID 22323654—
ReactantHCID 178418361HCID 178418361—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-(3-Azidopropoxy)-2,6-dihydroxymethylpyridineHCID 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 (MgSO4) and concentrated in vacuo. The resultant residue was purified by silica gel flash column chromatography to give the title compound. 1H NMR (DMSO) δ2.00 (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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559303B1
Source datasetuspto-grants-2003_05
ORD IDord-5055990994a944c78e026e88efe726f5
Source noteuspto-grants-2003_05