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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452042Generated: October 30, 2026

Hydrochloric Acid → HCID 19973434, compound

https://huagongshe.com/reaction/1452042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantEthyl BromideHCID 6332—
ReactantMagnesiumHCID 5462224—
Reactant6-Bromo-2-methylimidazo[1,2-a]pyridineHCID 12428960—
CatalystIodineHCID 807—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19973434HCID 1997343491.9%

Reaction Steps

In a nitrogen atmosphere, 78.56 g of magnesium was added to 2 l of tetrahydrofuran and 0.3 g of iodine and 18 ml of bromoethane were added to the obtained mixture to prepare a Grignard reagent. A solution of 170.5 g of 6-bromo-2-methylimidazo[1,2-a]pyridine and 162 ml of bromoethane in 500 ml of tetrahydrofuran was slowly dropped into the above reaction mixture. After the completion of the dropping, the obtained mixture was heated under reflux for 30 minutes and then cooled with ice. Formaldehyde gas generated by heating a container containing 242 g of paraformaldehyde to 200° C. was introduced into the reaction mixture by the use of a nitrogen stream. After 30 minutes, dilute hydrochloric acid was added to the resulting mixture and the obtained mixture was filtered to remove insolubles. The filtrate was alkalinized with concentrated aqueous ammonia and extracted with chloroform. The organic phase was dried over anhydrous magnesium sulfate and distilled to remove the solvent. The residue was purified by silica gel column chromatography [solvent: dichloromethane/methanol (30:1 to 10:1)] to give 120 g of the title compound as a pale-yellow solid (yield: 91.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05606061
Source datasetuspto-grants-1997_02
ORD IDord-29559e7c5f4c41a186cfca5243451495
Source noteuspto-grants-1997_02