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Hydrochloric Acid → Atomoxetine Hydrochloride

HRID 2116884
Notes
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Reaction equation

HRID 2116884 reaction equation
[ClH:1].[CH3:2][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:8]=1[O:9][C@@H:10]([C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1)[CH2:11][CH2:12][NH:13][CH3:14]>>[CH3:2][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:8]=1[O:9][C@@H:10]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH2:11][CH2:12][NH:13][CH3:14].[ClH:1]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 313Hydrochloric AcidHCID 54841Atomoxetine

Product 1

HCID 54840Atomoxetine Hydrochloride

Procedure

Under stirring, and maintaining temperature between 18° C. and 20° C. by means of water bath cooling, 3.27 g (0.03263 mol) of aqueous hydrogen chloride (36.4%) was dropped on 58.2 g (0.02967 mol) of the atomoxetine base solution obtained above. Atomoxetine hydrochloride then crystallized out. The obtained suspension was stirred at about 20° C. for one hour, the solid is collected by filtration, and washed twice with 6 ml of n-butyl acetate. The solid was collected and dried for 18 hours at 45° C. under vacuum.

Workup

  1. temperaturemaintaining temperature between 18° C. and 20° C. by means of water bath
  2. temperaturecooling
  3. customobtained above
  4. customAtomoxetine hydrochloride then crystallized out
  5. stirring
The obtained suspension was stirred at about 20° C. for one hour
  • filtrationthe solid is collected by filtration
  • washwashed twice with 6 ml of n-butyl acetate
  • customThe solid was collected
  • customdried for 18 hours at 45° C. under vacuum
  • Sources & evidence

    ORD record
    ord-b5f5f8d6c3a742a4bd5b3dbc5d1c308a
    Source dataset
    uspto-grants-2008_10
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07439399B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes