Reaction equation
[CH3:1][NH:2][C@@H:3]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[C@H:6]([C:13]2[CH:14]=[CH:15][C:16]([Cl:20])=[C:17]([Cl:19])[CH:18]=2)[CH2:5][CH2:4]1.[ClH:21]>C(O)CCCCC>[CH3:1][NH:2][C@@H:3]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[C@H:6]([C:13]2[CH:14]=[CH:15][C:16]([Cl:20])=[C:17]([Cl:19])[CH:18]=2)[CH2:5][CH2:4]1.[ClH:21]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 50.8 g free sertraline base in 100 ml of n-hexanol was added dropwise over a period of about 30 minutes at room temperature onto 100 ml of n-hexanol containing 14 ml of 37% aqueous hydrochloric acid. About ¾ of the way through the addition a white crystalline solid starts to form. Stirring is maintained for 1 hour then the solid is filtered and washed. It is dried under vacuum. 49.5 g of sertraline hydrochloride form II are obtained in a yield of 87%.
Workup
- additionAbout ¾ of the way through the addition a white crystalline solid starts
- customto form
- temperatureis maintained for 1 hour
- filtrationthe solid is filtered
- washwashed
- customIt is dried under vacuum
Sources & evidence
- ORD record
- ord-2b79fac7a43a4e7aa04375394eda4583
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07173153B2
Linked notes
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