Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 18928733 | HCID 18928733 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 18928715 | HCID 18928715 | — |
Reaction Steps
A solution of thionyl chloride (15.7 ml) in dry chloroform (100 ml) was added dropwise to a stirred solution of the product from Example 35 (51.1 g) in dry chloroform (500 ml) over 45 minutes, keeping the temperature between 0° C. and 5° C. The solution was allowed to warm to 20° C. with stirring and then heated under reflux for 2.5 hours. The mixture was cooled to 20° C., washed (saturated sodium bicarbonate solution, water), dried, filtered and evaporated to give 4-(2-chloroethyl)-1-(3-phenylpropionyl)piperidine as oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05741800 |
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| Source dataset | uspto-grants-1998_04 |
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| ORD ID | ord-a3a1819e3bba428eb7d039474baaaaf8 |
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| Source note | uspto-grants-1998_04 |
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