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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397248Generated: October 29, 2026

Hydrochloric Acid → HCID 9992929, compound

https://huagongshe.com/reaction/397248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantL-LeucineHCID 6106—
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantHCID 23666323HCID 23666323—
ReactantHCID 23669769HCID 23669769—
ReactantSodium cyclohexanecarboxylateHCID 23673627—
SolventSodium HydroxideHCID 14798—
ProductHCID 9992929HCID 999292977%

Reaction Steps

Cyclohexanoyl chloride (32.7 mL, 232 mmole) was added dropwise to a solution of (L)-leucine (37 g, 282 mmole) in aqueous sodium hydroxide (500 mL, 2 N). During the course of this addition, the reaction temperature was maintained below 45° C. using an ice/water bath, as necessary. The pH was maintained at about 10 by the addition of aliquots of 14 N NaOH, as necessary. After the addition was complete, the reaction mixture was stirred for an additional 2 hours at room temperature. The resulting clear solution was adjusted to pH 2.5 by the dropwise addition of concentrated hydrochloric acid. The precipitate was collected by filtration, re-dissolved in a minimum amount of 12 N sodium hydroxide, and re-precipitated by dropwise addition of concentrated hydrochloric acid and filtered. The crude reaction product was a white solid and contained about 85% N-cyclohexanoyl leucine sodium salt, about 10% cyclohexane carboxylic acid sodium salt, and about 5 N-cyclohexanoylleucylleucine sodium salt, by weight. The solid was washed with dilute aqueous hydrochloric acid (750 mL, 0.1 N) to provide N-cyclohexanoyl-(L)-leucine as a white crystalline solid (52.6 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610329B2
Source datasetuspto-grants-2003_08
ORD IDord-7cd8b7b474994630abff1563e7f9aad8
Source noteuspto-grants-2003_08