HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54964Erstellt: 25. Oktober 2026
Potassium Chloride → 1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thione
https://huagongshe.com/reaction/54964
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Chloride | HCID 4873 | — |
| Edukt | Carbon Disulfide | HCID 6348 | — |
| Edukt | Potassium Acetate | HCID 517044 | — |
| Edukt | Carbamodithioic acid | HCID 3001860 | — |
| Edukt | 2-[(Methylamino)methyl]-alpha-phenylbenzenemethanamine dihydrochloride | HCID 19957059 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | 1,2,4,5-Tetrahydro-4-methyl-1-phenyl-3H-2,4-benzodiazepin-3-thione | HCID 14978307 | 38% |
Reaktionsschritte
To a suspension of 15 g (50 mmol) of 2-[(methylamino)methyl]-α-phenylbenzenemethanamine dihydrochoride in 100 mL of isopropyl alcohol was added 10 g (100 mmol) of potassium acetate followed by 3.3 mL (55 mmol) of carbon disulfide in 35 mL of isopropyl alcohol. The suspension was stirred at room temperature for one and one-half hours and then refluxed for 30 minutes. The reaction was chilled in ice and the internal salt of the carbamodithioic acid, contaminated with two equivalents of of potassium chloride, was filtered off. The carbamodithioic acid was suspended in 125 mL of 95% ethanol, and 1.3 mL of of 12N hydrochloric acid was added. The suspension was refluxed for three days, cooled, and 15.3 g (114%) of the crude benzodiazepin-3-thione was filtered off. A 6-g portion of the crude product was recrystallized from 2-ethoxy ethanol to yield 2.0 g (38%) of product, mp 208-209.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05624922 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-2068da37eed34df5b6bdbddc2bfafcbc |
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| Quellennotiz | uspto-grants-1997_04 |
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