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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881857Generated: November 2, 2026

Dimethyl Sulfoxide → 5-(1,2-Dihydroxy-2-methylpropyl)pyridine-2-carbaldehyde

https://huagongshe.com/reaction/1881857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(2-Methylprop-1-en-1-yl)pyridine-2-carbaldehydeHCID 46941436—
Product5-(1,2-Dihydroxy-2-methylpropyl)pyridine-2-carbaldehydeHCID 5933148879%

Reaction Steps

To a solution of 5-(2-methylprop-1-en-1-yl)pyridine-2-carbaldehyde (9.40 g) in a mixed solvent of dimethylsulfoxide (230 mL) and water (1.89 mL) was added N-bromosuccinimide (18.7 g) at 0° C. The reaction solution was warmed to room temperature and stirred at room temperature for 1 hr. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed successively with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. To a solution of the residue in tetrahydrofuran (200 mL) was added 4.5M aqueous sulfuric acid solution, and the mixture was stirred at room temperature for 3 hr. The reaction mixture was neutralized with aqueous sodium hydroxide solution and saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed successively with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=20:80-100:0, volume ratio) to give the title compound (9.00 g, yield 79%) as a pale-yellow oil. MS: 196 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318746B2
Source datasetuspto-grants-2012_11
ORD IDord-2fdb26b668b04688bb776366497616c7
Source noteuspto-grants-2012_11