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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438422Generated: October 27, 2026

2-Methyl-3-butyn-2-ol → 4-(5-Chloro-3-nitro-pyridin-2-yl)-2-methyl-but-3-yn-2-ol

https://huagongshe.com/reaction/1438422

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-3-butyn-2-olHCID 8258—
ReactantTriethylamineHCID 8471—
Reactant2-Bromo-5-chloro-3-nitropyridineHCID 280681—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product4-(5-Chloro-3-nitro-pyridin-2-yl)-2-methyl-but-3-yn-2-olHCID 57942532—

Reaction Steps

To a mixture of 2-bromo-5-chloro-3-nitro-pyridine (2.5 g, 10.6 mmol), Cul (141 mg, 0.74 mmol), Pd(PPh3)4, (367 mg, 0.32 mmol) and 2-Methyl-3-butyn-2-ol (1.5 mL, 15.8 mmol) was added 1-methyl-2-pyrorolidone (20 mL) followed by Et3N (6 mL, 22 mmol). After stirring for 4 h 30 min at room temperature, the reaction mixture was poured into water (20 mL) and extracted with EtOAc (3×30 mL). The combined organic extracts were washed with brine (20 mL), dried (Na2SO4), filtered and concentrated under reduced pressure, and the residue was purified by flash column chromatography over silica gel (EtOAc/Hexanes, 2:98, then 5:95) to provide 4-(5-chloro-3-nitro-pyridin-2-yl)-2-methyl-but-3-yn-2-ol. MS m/z: 241.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622583B2
Source datasetuspto-grants-2009_11
ORD IDord-d3c4be5a9a5041a8b215cc5d3d36e9c2
Source noteuspto-grants-2009_11