HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzaldehyde → HCID 20528326, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzaldehyde | HCID 240 | — |
| Edukt | Potassium Cyanide | HCID 9032 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | 1,3-Diazepane-2-thione | HCID 736589 | — |
| Edukt | 2-Thienyl-alpha-hydroxybenzyl ketone | HCID 54002001 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | HCID 20528326 | HCID 20528326 | — |
Reaktionsschritte
A mixture of 9.2 ml. of thiophene-2-carboxyaldehyde, 8 g. of potassium cyanide and 10.1 ml. of benzaldehyde in 100 ml. of 65% ethanol is reacted as described in Example 20, giving 6.2 g. of 2-thienyl-α-hydroxybenzyl ketone. A 4.36 g. portion of this ketone is reacted with methanesulfonyl chloride as described in Example 20, giving 3.2 g. of the methanesulfonate ester. A 2.64 g. portion of this ester and 1.30 g. of hexahydro-2H-1,3-diazepine-2-thione in 100 ml. of acetone are allowed to stand 48 hours, the solid is collected, washed with ether and dried in vacuo, giving 2.8 g. of the desired product, m.p. 149°-151° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04344954 |
| Quelldatensatz | uspto-grants-1982_08 |
| ORD ID | ord-34472b1a55034bc2a3b0726c4608e611 |
| Quellennotiz | uspto-grants-1982_08 |