HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sinapic acid → HCID 178490513, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sinapic acid | HCID 10743 | — |
| Edukt | Diethyl chlorophosphate | HCID 13139 | — |
| Edukt | 3-[4-(Acetyloxy)-3,5-dimethoxyphenyl]prop-2-enoic acid | HCID 53661480 | — |
| Edukt | HCID 178483797 | HCID 178483797 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | HCID 178490513 | HCID 178490513 | — |
Reaktionsschritte
Using 2.9 g of 4-acetoxy-3,5-dimethyoxycinnamic acid derived from 3,5-dimethoxy-4-hydroxycinnamic acid by the acetylation thereof, 2.8 ml of diethyl chlorophosphate, 2.7 ml of triethylamine, 100 ml of methylene chloride, 3 ml of N-(2-dimethylaminoethyl)-trans-4-methylcyclohexylamine (Example 78), and 0.5 g of 4-dimethylaminopyridine, a reaction similar to that conducted in Example 75 was carried out. As a result, 1.95 g of N-(2-dimethylaminoethyl)-N-(trans-4-methylcyclohexyl)-3,5-dimethoxy-4-hydroxycinnamamide (a compound of the present invention) was obtained as a pale yellow oil, which had the following physiochemical properties:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05344845 |
| Quelldatensatz | uspto-grants-1994_09 |
| ORD ID | ord-6a41895f3597499abb3902f25d1cc03e |
| Quellennotiz | uspto-grants-1994_09 |