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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | 6-tert-Butyl-2-(3,3-dimethylbut-1-ynyl)nicotinonitrile | HCID 67996132 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Tert-butyl-2-(3,3-dimethylbut-1-ynyl)nicotinaldehyde | HCID 86680254 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273080B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-814602ba4ae84b7aafabde5aff5e0484 |
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| Source note | uspto-grants-2016_03 |
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