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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223520Generated: October 26, 2026

Pyridine → 2-Methyl-3-hydroxy-4-acetyl-5-vinylpyridine

https://huagongshe.com/reaction/223520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Methyl-3-hydroxy-4-(1-hydroxyethyl)-5-vinylpyridineHCID 20263921—
Catalystchromium (VI) trioxideHCID 10219390—
SolventDichloromethaneHCID 6344—
Product2-Methyl-3-hydroxy-4-acetyl-5-vinylpyridineHCID 20264046—

Reaction Steps

To 750 ml. of dry methylene chloride containing 47.5 ml. of dry pyridine was added with stirring and cooling 29.6 g. of chromium trioxide. The mixture was aged 20 minutes at room temperature and then treated with a solution of 10.96 g. of the product from Example 10, Step B, in 250 ml. of dry methylene chloride over 15 minutes. After one hour at room temperature, the reaction mixture was filtered and the residue was washed with 2×100 ml. of methylene chloride. The methylene chloride filtrates were extracted with 3×500 ml. of 5% (w/w) aqueous sodium hydroxide solution, dried over magnesium sulfate and evaporated to dryness. The residue was crystallized from hexane to give 2-methyl-3-hydroxy-4-acetyl-5-vinylpyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04355034
Source datasetuspto-grants-1982_10
ORD IDord-dad867cda2cc407698337b6a4bca0553
Source noteuspto-grants-1982_10