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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638307Generated: October 31, 2026

Pyridine → HCID 12674764, compound

https://huagongshe.com/reaction/638307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant1-(2-Hydroxyethyl)pyrroleHCID 10975438—
SolventWaterHCID 962—
ProductHCID 12674764HCID 1267476455%

Reaction Steps

The resulting product is reacted with acetic anhydride in accordance with the method of F. F. Blicke and E. S. Blake, J. Am. Chem. Soc., 53, 1015(1931). A mixture of 1-(2-hydroxyethyl)pyrrole (147 g, 1.32 mole), pyridine (415 ml) and acetic anhydride (139 ml) is heated on a steam bath for 0.5 hours. The reaction mixture is cooled to room temperature, poured into water (one l) and the product is extracted into ethyl acetate (3×1 l ). The extract is washed successively with dilute hydrochloric acid, saturated sodium chloride solution, dilute sodium bicarbonate solution, and again with saturated sodium chloride solution. The extract is dried over sodium sulfate, evaporated in vacuo and the residue (150 g) is subjected to column chromatography on Florisil® activated magnesium silicate. The desired product is eluted with hexane-dichloromethane (1:1) to give 128 g (55%) 1-(2-acetoxyethyl)pyrrole, an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04560699
Source datasetuspto-grants-1985_12
ORD IDord-d10057da72b54615931db0b4cba4f144
Source noteuspto-grants-1985_12