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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654952Generated: October 30, 2026

Pyridine → HCID 15723380, compound

https://huagongshe.com/reaction/654952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 15723379HCID 15723379—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15723380HCID 15723380—

Reaction Steps

To 4-(1-acetoxy-9-hydroxynonyl)-2-trimethylsilylfuran (0.075 g, 0.221 mmol) and pyridine (0.056 g, 0.662 mmol) in tetrahydrofuran (2 ml) under argon at 0° was added dropwise acetyl chloride (0.052 g, 0.662 mmol). The mixture was warmed to room temperature, stirred for one hour, quenched with water and extracted into ethyl ether. The organic portion was washed with 10% hydrochloric acid, saturated sodium bicarbonate, aqueous 5% cupric sulfate solution, water, saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to an oil. Purification by flash chromatography (silica, 5 to 10% ethyl acetate/hexane) gave the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05134128
Source datasetuspto-grants-1992_07
ORD IDord-447c0ed11a99485c99504677fd87a9b4
Source noteuspto-grants-1992_07