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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494136Generated: October 31, 2026

Pyridine → HCID 10342851, compound

https://huagongshe.com/reaction/1494136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 86744863HCID 86744863—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 10342851HCID 10342851—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 1.44 g of 8-(p-chlorophenylsulfonamido-4-[3-(3-pyridyl)-propyl]-octanamide and 0.52 mL pyridine in 5.8 mL dioxane is cooled to 0° C. and 0.51 mL trifluoroacetic anhydride is added over a period of 1 hour. The mixture is then stirred at room temperature for 3 hours. The reaction is quenched by the addition of saturated aqueous sodium bicarbonate solution and extracted with methylene chloride (2×20 mL). The combined organic extracts are dried, filtered and evaporated to give 8-(p-chlorophenyl- sulfonamido)-4-[3-(3-pyridyl)propyl]octanenitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025025
Source datasetuspto-grants-1991_06
ORD IDord-a30b9d772ad84bc7b58c937cad95486f
Source noteuspto-grants-1991_06