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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921044Generated: October 30, 2026

Sulfuric Acid → 6-Tert-butyl-2-(3,3-dimethylbut-1-ynyl)nicotinaldehyde

https://huagongshe.com/reaction/921044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant6-tert-Butyl-2-(3,3-dimethylbut-1-ynyl)nicotinonitrileHCID 67996132—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product6-Tert-butyl-2-(3,3-dimethylbut-1-ynyl)nicotinaldehydeHCID 86680254—

Reaction Conditions

Temperature-78 °C

Reaction Steps

310 ml (315 mmol) of diisobutylaluminium hydride, 1M in toluene, are added dropwise to a solution, cooled to −78° C., of 72.1 g (300 mmol) of 6-tert-butyl-2-(3,3-dimethylbut-1-ynyl)nicotinonitrile, S62, in 1500 ml of dichloromethane at such a rate that the temperature does not exceed −65° C. When the addition is complete, the reaction mixture is stirred at −78° C. for a further 2 h, then allowed to warm slowly to room temperature and stirred for a further 12 h. After re-cooling to −10° C., 300 ml of THF and then, with vigorous stirring, 400 ml of 2 N sulfuric acid (exothermic!) are added, and the mixture is stirred at room temperature for a further 12 h. After re-cooling to −10° C., a solution of 70 g of NaOH in 300 ml of water is added, the aqueous phase is separated off, the organic phase is washed three times with 1000 ml of water each time, once with 500 ml of saturated sodium chloride solution, dried over magnesium sulfate, and the solvent is removed in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273080B2
Source datasetuspto-grants-2016_03
ORD IDord-814602ba4ae84b7aafabde5aff5e0484
Source noteuspto-grants-2016_03