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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956119Generated: November 2, 2026

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

https://huagongshe.com/reaction/1956119

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) 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780241
Source datasetuspto-grants-1998_07
ORD IDord-2e021bfd617d41e3bc72fc8320b3dc03
Source noteuspto-grants-1998_07