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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284059Generated: October 29, 2026

Benzyl Alcohol → HCID 21515609, compound

https://huagongshe.com/reaction/1284059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHCID 21515601HCID 21515601—
CatalystSulfuric AcidHCID 1118—
ProductHCID 21515609HCID 21515609—

Reaction Steps

4 g. of 2,6-dimethyl-3,5-dicarboethoxy-N-phenyl-4-pyridone (prepared as described in Example 1) were dissolved in 20 ml. of benzyl alcohol, 4 drops of concentrated H2SO4 were added and the mixture was stirred and heated for 7 hours at 130°, at the same time distilling off the produce ethanol. The benzyl alcohol solution was washed with a saturated solution of sodium bicarbonate and the slurry was extracted several times with chloroform. The extracts were combined and dried over magnesium sulphate, and the chloroform was distilled off in vacuo. The oily residue was dissolved in 50 ml. of ether and 50 ml. of petrolether 40'-60° were added. After cooling in a dry ice-acetone bath and scratching, 2,5g. of 2,6-dimethyl-3-carboethoxy-5-carbobenzyloxy-N-phenyl-4-pyridone, m.p. 142° were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03978072
Source datasetuspto-grants-1976_08
ORD IDord-3bfbf5e297a449428184f4f3b52f5f20
Source noteuspto-grants-1976_08