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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243795Generated: October 29, 2026

Hydrochloric Acid → HCID 23133647, compound

https://huagongshe.com/reaction/243795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
ReactantDiisobutylammonium hydrideHCID 21898182—
ReactantHCID 23133650HCID 23133650—
SolventDichloromethaneHCID 6344—
ProductHCID 23133647HCID 23133647—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653277B2
Source datasetuspto-grants-2014_02
ORD IDord-8aca73b1644b4d12bebcfad250fd12e8
Source noteuspto-grants-2014_02