HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 590954Erstellt: 26. Oktober 2026
Toluene → ethyl 2-hydroxy-2-(1-methyl-3-phenyl-1H-indol-2-yl)acetate
https://huagongshe.com/reaction/590954
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Ethyl oxoacetate | HCID 70211 | — |
| Edukt | 1-Methyl-3-phenylindole | HCID 610176 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | ethyl 2-hydroxy-2-(1-methyl-3-phenyl-1H-indol-2-yl)acetate | HCID 70813741 | 22% |
Reaktionsschritte
A solution of butyllithium (1.6 M, 3.44 mL, 5.5 mmol) was added at −20° C. to a solution of 1-methyl-3-phenyl-1H-indole (1b) (1.08 g, 5.3 mmol) in anhydrous tetrahydrofuran (20 mL) under a nitrogen atmosphere. After 1 hour, a solution of ethyl glyoxylate in toluene (50%, 1.1 mL, 5.5 mmol) was added. The reaction mixture was slowly warmed to room temperature for 2 hours, quenched with water (5 mL) and concentrated in vacuo. The residue was partitioned between dichloromethane (40 mL) and water (15 mL). The organic layer was washed with water (2×15 mL), brine (15 mL), dried over sodium sulfate, filtered and evaporated to dryness. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 90/10) to afford the desired alcohol (1c) as a white solid (360 mg, 1.16 mmol, 22%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US09238026B2 |
|---|
| Quelldatensatz | uspto-grants-2016_01 |
|---|
| ORD ID | ord-a240b766312c4329a26c1b3ed43fb300 |
|---|
| Quellennotiz | uspto-grants-2016_01 |
|---|