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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881838Generated: November 2, 2026

Sodium borohydride → 1-(6-Bromopyridin-3-yl)ethane-1,2-diol

https://huagongshe.com/reaction/1881838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 2-(6-bromopyridin-3-yl)-2-oxoacetateHCID 46941438—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product1-(6-Bromopyridin-3-yl)ethane-1,2-diolHCID 4694143777%

Reaction Steps

To a solution of ethyl (6-bromopyridin-3-yl)(oxo)acetate (1.00 g) in ethanol (20 mL) was slowly added sodium borohydride (250 mg). The reaction mixture was stirred at room temperature for 4 hr, diluted with ethyl acetate and washed with water. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated to give the title compound (650 mg, yield 77%) as a colorless oil. MS: 220 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318746B2
Source datasetuspto-grants-2012_11
ORD IDord-acb1dd40ca2249f98f12b42aa3d02dc3
Source noteuspto-grants-2012_11