Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Ethyl 4-(2-(4-tolylsulfanyl)phenyl)-piperidin-1-carboxylate | HCID 45258309 | — |
| Product | Tedatioxetine Hydrobromide | HCID 24751582 | — |
Reaction Steps
The crude ethyl 4-(2-(4-tolylsulfanyl)phenyl)-piperidin-1-carboxylate as a red oil from example 3 was mixed in a stirred reactor with hydrobromic acid in acetic acid (40%, 545 mL, 3.11 mol). The mixture was heated at 80° C. for 18 hours. The reaction mixture was cooled down to room temperature. During the cooling the product crystallises out. After 1 hour at room temperature ethyl ether (800 mL) was added to the reaction mixture, and the mixture was stirred for another hour. The product was filtered off, washed with ethyl ether and dried in a vacuum oven at 50° C. until constant weight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507526B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-c8b227c8ee454fb7844e9c727f2f7f24 |
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| Source note | uspto-grants-2013_08 |
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