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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386063Generated: October 25, 2026

Sodium borohydride → 2-[4-(6-Bromopyridin-2-yl)-1H-1,2,3-triazol-1-yl]ethanol

https://huagongshe.com/reaction/386063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactantethyl[4-(6-bromopyridin-2-yl)-1H-1,2,3-triazol-1-yl]acetateHCID 59525977—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-[4-(6-Bromopyridin-2-yl)-1H-1,2,3-triazol-1-yl]ethanolHCID 59526312—

Reaction Steps

To a solution of NaBH4 (60 mg, 1.58 mmol) in MeOH (3.0 mL) at room temperature was added ethyl[4-(6-bromopyridin-2-yl)-1H-1,2,3-triazol-1-yl]acetate (245 mg, 0.79 mmol) in MeOH (7.0 mL) The reaction was stirred at room temperature for 2 h. It was then diluted with water and extracted with EtOAc (2×). The combined organic layers were washed with brine, dried (MgSO4), filtered, and evaporated. Flash chromatography (20-100% EtOAc/hexanes) afforded the title compound as a colorless gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-37c3845d1eeb4d459582c137cdd8120d
Source noteuspto-grants-2013_02