HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Vinylidene chloride → Ethyl 5-chloro-1,2-oxazole-3-carboxylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Vinylidene chloride | HCID 6366 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ethyl 2-chloro-2-(hydroxyimino)acetate | HCID 6399471 | — |
| Produkt | Ethyl 5-chloro-1,2-oxazole-3-carboxylate | HCID 66831968 | 35% |
Reaktionsschritte
To a solution of ethyl chlorooximidoacetate (11.0 g, 72.6 mmol, 1 equiv) in 1,1-dichloroethylene (350 mL) was added Et3N (25.3 mL, 181 mmol, 2.5 equiv) in 1,1-dichloroethylene (100 mL) via addition funnel over 30 min. The reaction mixture was stirred at room temperature for 23 h, then was partitioned between water (150 mL) and CH2Cl2 (2×150 mL). The combined organic layers were dried over Na2SO4 and were concentrated. The residue was purified by flash column chromatography (10% EtOAc in hexanes) to give the title intermediate (4.49 g, 35%) as a pale yellow oil: IR (cm−1) 1735, 1436, 1253; 1H NMR (CDCl3) δ 1.45 (t, 3H, J=7.2), 4.49 (q, 2H, J=7.2), 7.29 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06514997B2 |
| Quelldatensatz | uspto-grants-2003_02 |
| ORD ID | ord-eee196f7069440a39edd9f046a80d4cb |
| Quellennotiz | uspto-grants-2003_02 |