HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50033Erstellt: 25. Oktober 2026
Dichloromethane → Ethyl 5-chloro-3-(3,5-dimeihylphenylthio)-6-fluoroindole-2-carboxylate
https://huagongshe.com/reaction/50033
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Boron trifluoride etherate | HCID 8000 | — |
| Edukt | N-(3,5-Dimethylphenylthio)succinimide | HCID 11053620 | — |
| Edukt | Ethyl 5-chloro-6-fluoro-1H-indole-2-carboxylate | HCID 11413806 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Sodium chloride; water | HCID 57417360 | — |
| Produkt | Ethyl 5-chloro-3-(3,5-dimeihylphenylthio)-6-fluoroindole-2-carboxylate | HCID 21301066 | 102,4% |
Reaktionsschritte
Boron trifluoride ethyl etherate (0.135 g, 0.12 mL, 0.001 mol) was added to a mixture of ethyl 5-chloro-6-fluoroindole-2-carboxylate (0.75 g, 0.0031 mol), N-(3,5-dimethylphenylthio)-succinimide (0.78 g, 0.0033 mol) and anhydrous dichloromethane (20 mL) under dry argon atmosphere. After stirring at room temperature for 2 hours was added boron trifluoride ethyl etherate (0.27 g, 0.24 mL, 0.002 mol) and then reaction was heated at 45° C. for 2 hours. After cooling reaction was diluted chloroform and brine while shaking. Organic layer was separated, washed with saturated solution of sodium hydrogen carbonate, then with brine and dried. The solvent was evaporated to give 1.2 g (100%) of satisfactory pure title compound, mp 170-173° C. (from ethanol).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06710068B2 |
|---|
| Quelldatensatz | uspto-grants-2004_03 |
|---|
| ORD ID | ord-72582ea7baff4f51bacbd7e698208507 |
|---|
| Quellennotiz | uspto-grants-2004_03 |
|---|