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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116842Generated: November 1, 2026

Hydrochloric Acid → Atomoxetine Hydrochloride

https://huagongshe.com/reaction/2116842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantAtomoxetineHCID 54841—
ReactantHCID 131727128HCID 131727128—
SolventWaterHCID 962—
SolventButyl AcetateHCID 31272—
ProductAtomoxetine HydrochlorideHCID 54840—

Reaction Steps

One mole of atomoxetine (S)-(+)-mandelate (88.6% w/w by potentiometric assay) was mixed under stirring with 2037.5 ml of n-butyl acetate and 2037.5 ml of water. Keeping the temperature between 20-25° C., 1.529 moles of 30% aqueous sodium hydroxide was added, and then the phases were separated. The organic phase was washed twice with 400 ml of water, then filtered on paper and used for the next step. While stirring and maintaining the temperature between about 22° C. and about 25° C. by means of water bath cooling, 1.1435 moles of aqueous hydrogen chloride (36%) was dropped on the atomoxetine base solution obtained above. The hydrochloride then crystallized. The obtained suspension was stirred at about 25° C. for one hour; the solid was collected by filtration, and washed twice with 345 ml of n-butyl acetate. The solid collected was dried for 18 hours at 70° C. under vacuum. Enantiomeric purities are summarized in the following table:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439398B2
Source datasetuspto-grants-2008_10
ORD IDord-a983424e5880433e80738a88fa06ca5c
Source noteuspto-grants-2008_10