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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738585Generated: October 26, 2026

Hydrochloric Acid → Salcaprozic acid

https://huagongshe.com/reaction/1738585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOctahydro-2H-azonin-2-oneHCID 13632—
ReactantSodium HydroxideHCID 14798—
Reactant8-Aminooctanoic acidHCID 66085—
Reactant2-Aminooctanoic acidHCID 69522—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductSalcaprozic acidHCID 158789—

Reaction Conditions

Temperature25 °C

Reaction Steps

Sodium hydroxide (1.68 g, 42.0 mmol, 1.2 eq), 2-azacyclononanone (5.0 g, 35.5 mmol, 1.0 eq) and 20 mL of water were placed a 100 mL round bottom flask equipped with a magnetic stir bar and cold water condenser to prepare aminocaprylic acid. The reaction mixture was heated to reflux for 2.5 hours (at which time the reaction was determined to have finished, by TLC) and cooled to 25 degrees C. A solution of oligosalicylate (4.87 g, 40 mmol, 1.1 eq) and dioxane (50 mL) was added to the aqueous solution of 8-aminocaprylic acid. This mixture was heated to reflux for 2.25 hours (at which time the reaction was determined to have finished, by HPLC). The clear orange reaction mixture was cooled to 25 degrees C. and acidified to pH=1 with 3% (by vol.) aqueous hydrochloric acid. All the dioxane and some of the water were stripped (60 degrees C., 50 min). The aqueous phase was decanted from the brown oil while still warm. Crystallization of the oil from ethanol-water yielded a white precipitate. The solid was recovered by filtration and was dried over 4 hours in a 50 degrees C. vacuum oven. The N-(salicyloyl)-8-aminocaprylic acid was isolated as a white solid (5.73 g, 59%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962710
Source datasetuspto-grants-1999_10
ORD IDord-9084a8a6b34f42c5abf487bd72bec8a6
Source noteuspto-grants-1999_10