HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 596497Erstellt: 24. Oktober 2026
Carbon Disulfide → alpha-(Nitromethyl)benzyl 1-piperidinecarbodithioate
https://huagongshe.com/de/reaction/596497
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbon Disulfide | HCID 6348 | — |
| Edukt | Beta-Nitrostyrene | HCID 7626 | — |
| Edukt | Piperidinium 1-piperidinecarbodithioate | HCID 2820349 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | alpha-(Nitromethyl)benzyl 1-piperidinecarbodithioate | HCID 11266906 | — |
Reaktionsschritte
β-Nitrostyrene (14.9 grams, 0.10 mole) was added in portions to a stirred mixture of piperidinium 1-piperidinecarbodithioate (24.6 grams, 0.10 mole), and carbon disulfide (7.6 grams, 0.10 mole) in methanol (200 ml.). During the addition, the reaction temperature was 25° C.-29° C. After the addition of β-nitrostyrene, the reaction mixture was cooled to 8° C., and the precipitated product was filtered off, washed with water, and dried in air. The yield of product melting at 85° C.-87° C. (prior sintering) was 29.0 grams (93%). Repeated recrystallizations without heating from methylene chloride-hexane and methylene chloride-methanol solutions gave pure α-(nitromethyl)benzyl 1-piperidinecarbodithioate melting at 86° C.-90.5° C. (prior sintering).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04011230 |
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| Quelldatensatz | uspto-grants-1977_03 |
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| ORD ID | ord-ae882f0193e946c4bdea7fcb06b2bf74 |
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| Quellennotiz | uspto-grants-1977_03 |
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