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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544474Generated: October 30, 2026

Sodium borohydride → 2-Methylimidazo[1,2-a]pyridine-8-methanol

https://huagongshe.com/reaction/544474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 13900241HCID 13900241—
SolventIsopropanolHCID 3776—
Product2-Methylimidazo[1,2-a]pyridine-8-methanolHCID 13900330—

Reaction Steps

To a stirred suspension of 56.8 g (0.36 mol) 2-methyl-8-formylimidazo[1,2-a]pyridine in 400 ml isopropanol at 0°is added in portions 8 g (0.21 mol) sodium borohydride. The reaction mixture is stirred at room temperature for an additional 2 hours. The excess sodium borohydride is decomposed by the addition of distilled waterand the solution concentrated under reduced pressure at 50° C. The residue is dissolved in water and extracted with chloroform. The chloroform extracts are combined and dried over anhydrous sodium sulfate. Following filtration, the chloroform is removed under reduced pressure to give 2-methyl-8-hydroxymethylimidazo[1,2-a]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04450164
Source datasetuspto-grants-1984_05
ORD IDord-0cd4031f60504719a0755472e7bc360a
Source noteuspto-grants-1984_05