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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521187Generated: October 30, 2026

2-Methyl-3-butyn-2-ol → HCID 86729354, compound

https://huagongshe.com/reaction/521187

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-3-butyn-2-olHCID 8258—
ReactantSodium AzideHCID 33557—
Reactant3-Bromobenzyl bromideHCID 69979—
ReactantSodium AscorbateHCID 23667548—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 86729354HCID 86729354—

Reaction Steps

To a solution of 1-bromo-3-(bromomethyl)benzene (5.0 g, 20 mmol) in DMSO (40 mL) was added sodium azide (1.3 g, 20 mmol). The resulting mixture was allowed to stir at ambient temperature for 18 hours before it was diluted with water and extracted with diethyl ether (2×). The combined organic extracts were washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The crude residue was dissolved in tBuOH (65 mL and water (39 mL) and to this mixture was added 2-methylbut-3-yn-2-ol (2.3 g, 27 mmol), and then a solution of copper (II) sulfate pentahydrate (0.26 g, 1.0 mmol) in water (10 mL) followed by a solution of sodium ascorbate (0.83 g, 4.2 mmol) in water (8 mL). The resulting mixture was allowed to stir at ambient temperature for 2 hours before it was diluted with water and extracted with EtOAc (2×). The combined organic extracts were washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The residue was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328099B2
Source datasetuspto-grants-2016_05
ORD IDord-0e740d2f93b847c0a224e383f3379aa5
Source noteuspto-grants-2016_05