HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzal chloride → Ethyl 1-(p-chlorobenzyl)-5-chloro-3-thiophenylindole-2-carboxylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzal chloride | HCID 7411 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Ethyl 5-chloro-3-thiophenylindole-2-carboxylate | HCID 67902874 | — |
| Edukt | Potassium hexamethylsilamide | HCID 131717145 | — |
| Katalysator | Tetrabutylammonium Bromide | HCID 74236 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexamethylphosphoramide | HCID 12679 | — |
| Produkt | Ethyl 1-(p-chlorobenzyl)-5-chloro-3-thiophenylindole-2-carboxylate | HCID 67855865 | — |
Reaktionsschritte
To a cold (-78°), stirred solution containing 664 mg of ethyl 5-chloro-3-thiophenylindole-2-carboxylate from Preparation 5 in 3.5 mL of dry tetrahydrofuran, under argon, was added 3.5 mL of a 0.62 M solution of potassium hexamethylsilamide in toluene. The reaction mixture was stirred at -78° for 1 h and at 0° for 1 h then recooled to -78°. 0.75 mL of g chlorobenzyl chloride, 1.0 mL of hexamethylphosphoric triamide and 20 mg of tetra-n-butylammonium bromide were then added. The resultant mixture was allowed to warm to room temperature and stirred for 18 h. Saturated aqueous ammonium chloride and ether were added. The ether layer was separated, washed with water, 10% aqueous cupric sulfate, water and brine and dried over MgSO4.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05225421 |
| Quelldatensatz | uspto-grants-1993_07 |
| ORD ID | ord-c149c78e537a4b2aaf0a44152e4574ab |
| Quellennotiz | uspto-grants-1993_07 |