Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | rac 7-Methoxy Lasofoxifene | HCID 11373717 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Lasofoxifene | HCID 216416 | — |
Reaction Steps
A mixture of cis-1-[2-[4-(6-methoxy-2-phenyl-1,2,3,4 tetrahydronaphthalen-1-yl)phenoxy] ethyl}pyrrolidine (12 g, 28 mmol), acetic acid (75 mL), and 48% HBr (75 mL) was heated at 100° C. for 15 h. The solution was cooled and the resulting white precipitate was collected by filtration. The hydrobromide salt (9.6 g, 69%) was dissolved in CHCl3/MeOH and was stirred with saturated NaHCO3 (aq). The layers were separated and the aqueous layer was further extracted with CHCl3/MeOH. The combined organic layers were dried (MgSO4), filtered, and concentrated to yield product as an off-white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07037530B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-d28f79854c6c4ab482df7cf5a4c5584a |
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| Source note | uspto-grants-2006_05 |
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