HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sodium ethoxide → Diethyl 2-dimethylamino-5-(2-methylbenzylthio)-2,4-hexadienedioate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Edukt | Ethyl (2-methylbenzylthio)acetate | HCID 13245059 | — |
| Edukt | N-(dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate | HCID 86743575 | — |
| Edukt | Diethyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioate | HCID 86743580 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Diethyl 2-dimethylamino-5-(2-methylbenzylthio)-2,4-hexadienedioate | HCID 53720386 | 72% |
Reaktionsschritte
The procedure is as in Example 2 for the preparation of diethyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioate, starting with N-(3-dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate (10 g), a 2M ethanolic solution of sodium ethylate (21 cc) and ethyl (2-methylbenzylthio)acetate (7.9 g) in ethanol (100 cc). After purification by chromatography on a silica column with a mixture of cyclohexane and ethyl acetate (70:30 by volume) as eluent, diethyl 2-dimethylamino-5-(2-methylbenzylthio)-2,4-hexadienedioate (9.5 g) is obtained in the form of a yellow oil, and is used in the crude state in the subsequent syntheses.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04886835 |
| Quelldatensatz | uspto-grants-1989_12 |
| ORD ID | ord-e6a5bd963247488d9dd60f39fd7d5c11 |
| Quellennotiz | uspto-grants-1989_12 |