HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243795Generated: October 29, 2026
Hydrochloric Acid → HCID 23133647, compound
https://huagongshe.com/reaction/243795
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Diisobutylammonium hydride | HCID 21898182 | — |
| Reactant | HCID 23133650 | HCID 23133650 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23133647 | HCID 23133647 | — |
Reaction Steps
2.47 g (13.5 mmol) of 5-chloro-3-cyano-4-methyl-2-methoxypyridine was dissolved in 50 ml of anhydrous dichloromethane, the solution was cooled to −78° C., and 20.3 ml (20.3 mmol) of a toluene solution of 1M diisobutylammonium hydride was dropwise added slowly. After stirring at −78° C. for two and a half hours, the temperature was gradually increased to room temperature, and stirring was carried out at the same temperature for three days. The obtained solution was cooled in an ice bath, and 30 ml of water was slowly added to terminate the reaction. The reaction mixture was poured into 150 ml of 1N hydrochloric acid, followed by extraction with 100 ml of dichloromethane twice. The dichloromethane solution was washed with 100 ml of a saturated sodium chloride solution and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain crude 5-chloro-3-formyl-4-methyl-2-methoxypyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653277B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-8aca73b1644b4d12bebcfad250fd12e8 |
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| Source note | uspto-grants-2014_02 |
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