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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881896Generated: October 26, 2026

Citric Acid → 1-(6-Bromopyridin-3-yl)-2-methoxyethanol

https://huagongshe.com/reaction/1881896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
Reactant1-(6-Bromopyridin-3-yl)-2-methoxyethan-1-oneHCID 59331558—
SolventEthanolHCID 702—
Product1-(6-Bromopyridin-3-yl)-2-methoxyethanolHCID 5933158096%

Reaction Steps

To a mixture of 1-(6-bromopyridin-3-yl)-2-methoxyethanone (15.85 g), tetrahydrofuran (15 mL) and ethanol (15 mL) was slowly added sodium borohydride (0.97 g) at room temperature, and the mixture was stirred at room temperature for 30 min. To the reaction mixture was added 10% aqueous citric acid solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was subjected to silica gel column chromatography, and the title compound (15.26 g, yield 96%) was obtained as a yellow oil from a fraction eluted with ethyl acetate. MS: 234 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318746B2
Source datasetuspto-grants-2012_11
ORD IDord-a5de980d5da344ef97f42271328f69f8
Source noteuspto-grants-2012_11