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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250840Generated: October 30, 2026

Acetic Acid → Atomoxetine Hydrochloride

https://huagongshe.com/reaction/2250840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant(S)-mandelic acidHCID 439616—
ReactantHCID 86602621HCID 86602621—
SolventTolueneHCID 1140—
ProductAtomoxetine HydrochlorideHCID 5484038.1%

Reaction Conditions

Temperature55 °C

Reaction Steps

To a suspension of (S)-(+)-mandelic acid (10.72 g; 0.070 mol) in water (10 ml) 9.86 g (0.0739 mol) of 30% aqueous sodium hydroxide were added and the mixture was heated to 50-60° C. until complete dissolution. The resulting clear aqueous solution was dropped over a solution of crude racemic tomoxetine acetate in toluene, obtained by addition of glacial acetic acid (7.40 g; 0.123 mol) to a solution in toluene of crude racemic tomoxetine (30 g, 0.117 mol, by HPLC assay), prepared on its turn as described in Example 1. During the addition, temperature was raised to 35° C.; the biphasic system was then heated under vigorous stirring to 40° C. and then it spontaneously cooled to 20° C. The resulting suspension was then stirred at 20° C. for one hour, filtered and washed twice with toluene (30 ml each). The solid was dried at 50° C. under vacuum. (R)-(−)-tomoxetine mandelate 18.24 g; enantiomeric ratio: R/S 97: 3 (by chiral HPLC). Yield: 38.1%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317127B2
Source datasetuspto-grants-2008_01
ORD IDord-81d3a30a4f044207bab47ff372688a87
Source noteuspto-grants-2008_01