HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethyl Thioglycolate → 2-(4,5-Diphenyl-1,3-oxazol-2-ylthio)acetic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethyl Thioglycolate | HCID 12185 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2-Chloro-4,5-diphenyloxazole | HCID 13131162 | — |
| Edukt | 2-Bromo-4,5-diphenyl-oxazole | HCID 21408706 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-(4,5-Diphenyl-1,3-oxazol-2-ylthio)acetic acid | HCID 722466 | — |
Reaktionsschritte
12 g. of thioglycolic acid ethyl ester is added to a suspension of 2.4 g. of NaH in 200 ml. of freshly distilled DMF, and the mixture is agitated until the evolution of hydrogen has ceased. Thereafter, 25.5 g. of 2-chloro-4,5-diphenyl-oxazole or 30 g. of 2-bromo-4,5-diphenyl-oxazole is added to the mixture. The latter is agitated for 5 hours at 80° and worked up as usual, thus obtaining the ethyl ester of 4,5-diphenyl-2-oxazolylmercaptoacetic acid, b.p. 207°-210°/0.1 mm.; m.p. 54°-56° (hexane).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04051250 |
| Quelldatensatz | uspto-grants-1977_09 |
| ORD ID | ord-e09b04154b454e03ae2e01d90bd3bfe6 |
| Quellennotiz | uspto-grants-1977_09 |