Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 2-Chlorothioxanthone | HCID 618848 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Edukt | 3-Chloroquinolizidine | HCID 20328834 | — |
| Katalysator | Ethyl Bromide | HCID 6332 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 20328821 | HCID 20328821 | — |
Reaktionsschritte
Several drops of ethyl bromide were added to a stirred suspension of 1.29 g. (0.054 g.-atom) of magnesium turnings in 5 ml. of tetrahydrofuran under a nitrogen atmosphere. After the reaction began 9.3 g. (0.054 mole) of 3-chloroquinolizidine in 100 ml. of tetrahydrofuran was added. After the addition was completed the mixture was stirred and refluxed for one hour and cooled to 0° C. To the chilled suspension of the Grignard reagent was added a solution of 12.55 g. (0.051 mole) of 2-chloro-9-thioxanthone in 300 ml. of tetrahydrofuran. The solution was stirred at 24° C. for two hours, poured into aqueous ammonium chloride and extracted with ether. The extracts were washed with water, dried and evaporated to give 2-chloro-9-(3-quinolizidinyl)-9-hydroxythioxanthene.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04089961 |
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| Quelldatensatz | uspto-grants-1978_05 |
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| ORD ID | ord-7e97f4f7917a405781fe469772573c1d |
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| Quellennotiz | uspto-grants-1978_05 |
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