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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892222Generated: October 31, 2026

Borane;tetrahydrofuran → HCID 58476618, compound

https://huagongshe.com/reaction/1892222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
ReactantHCID 58476590HCID 58476590—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58476618HCID 5847661846%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 3-(5-bromo-2-methoxypyridin-3-yl)-N,N-dimethylpropanamide (1.0 g, 3.0 mmol) in THF (40 mL) was added borane-tetrahydrofuran (1.0 M in THF, 8.71 mL) slowly. The reaction mixture was allowed to stir for 3 h at 50° C. The mixture was allowed to cool to rt and then concentrated to dryness. To the residue, a solution of HCl (3.0 M in water, 40 mL) was added. The resulting mixture was allowed to stir for 2 h at 80° C. The mixture was allowed to cool to rt and then was basified to pH>10 with a potassium hydroxide solution. The aqueous solution was extracted with DCM. The organic solutions were combined, washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography to give 3-(5-bromo-2-methoxypyridin-3-yl)-N,N-dimethylpropan-1-amine (0.377 g, 40%) as an oil. LCMS (FA): Rt=1.03 min, m/z=273.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507667B2
Source datasetuspto-grants-2013_08
ORD IDord-049de87442e44cd690f3aa866e97b1cd
Source noteuspto-grants-2013_08