HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrochloric Acid → HCID 20528316, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Benzoin | HCID 8400 | — |
| Edukt | Piperonal | HCID 8438 | — |
| Edukt | Potassium Cyanide | HCID 9032 | — |
| Edukt | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Edukt | 1,3-Diazepane-2-thione | HCID 736589 | — |
| Edukt | HCID 54204893 | HCID 54204893 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | HCID 20528316 | HCID 20528316 | — |
Reaktionsschritte
A mixture consisting of 12 g. of piperonal 8.4 ml. of p-fluorobenzaldehyde, 6 g. of potassium cyanide, and 80 ml. of 65% ethanol is reacted as described in Example 20, giving 11.7 g. of 4'-fluoro-3,4-methylenedioxybenzoin as an uncrystallizable oil. 9.0 g. of this benzoin is converted to its methanesulfonate ester by the procedure of Example 20, yielding 9.8 g. of ester as an uncrystallizable oil. The reaction of 4.9 g. of the crude methanesulfonate ester, and 1.16 g. of hexahydro-2H-1,3-diazepin-2-thione in 80 ml. of acetone, followed by treatment with 5 ml of 2 N ethanolic hydrogen chloride gives the title compound melting at 211°-213° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04344954 |
| Quelldatensatz | uspto-grants-1982_08 |
| ORD ID | ord-ba8adce569ad490c9586f19986e695ad |
| Quellennotiz | uspto-grants-1982_08 |