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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295395Generated: November 1, 2026

Hydrochloric Acid → HCID 20475365, compound

https://huagongshe.com/reaction/2295395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 20475368HCID 20475368—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
ProductHCID 20475365HCID 20475365—

Reaction Steps

1.4 g (5.8 mmols) of 3-methyl-6-acetoxymethyl-2,2'-bipyridine are boiled under reflux for 30 minutes in a mixture of 20 ml of 10% sodium hydroxide solution and 15 ml of ethanol. After cooling, the mixture is acidified with hydrochloric acid and washed with twice 20 ml of ethyl acetate. The aqueous phase is rendered alkaline with potassium carbonate, and the reaction product is extracted with 40 ml of ethyl acetate. After drying over sodium sulfate and concentration in vacuo, the 3-methyl-6-hydroxymethyl-2,2'-bipyridine is crystallised from diethyl ether. Yield: 0.99 g (85% of theory); melting point 51°-53° C. UV absorption (in chloroform): λmax =281 nm (ε=9400).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04424359
Source datasetuspto-grants-1984_01
ORD IDord-154de8da489945edbee2068994b2c872
Source noteuspto-grants-1984_01