HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Triethylamine → 4-Ethyl-3-o-chlorobenzoyl-4-oxazolin-2-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-Chlorobenzoyl chloride | HCID 69110 | — |
| Edukt | 4-Ethyloxazol-2(3H)-one | HCID 21322953 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 4-Ethyl-3-o-chlorobenzoyl-4-oxazolin-2-one | HCID 21322955 | — |
Reaktionsschritte
A solution of o-chlorobenzoyl chloride (1.93 g.) and 4-ethyl-4-oxazolin-2-one (1.13 g.) in 30 ml. of benzene is cooled to 10° C. and reacted with 1.21 g. of triethylamine dissolved in 5 ml. of benzene. The reaction mixture is stirred at room temperature for 1 hour. The excess triethylamine and benzene is removed under reduced pressure to leave a light yellow oil (2.4 g.) which is triturated with ethanol whereupon a crystalline solid separates. The solid is removed and washed with a small amount of cold ethanol and dried. Yield 0.3 g.; m.p. 110°-112° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04150030 |
| Quelldatensatz | uspto-grants-1979_04 |
| ORD ID | ord-b8b94529bf3a4d078af2c164c5aa785e |
| Quellennotiz | uspto-grants-1979_04 |