HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21006Erstellt: 23. Oktober 2026
Dimethylformamide → 4-Chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone
https://huagongshe.com/de/reaction/21006
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Edukt | 3-chloro-N-(1-methyl-1-phenylethyl)benzamide | HCID 47444761 | — |
| Edukt | HCID 178444656 | HCID 178444656 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-Chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone | HCID 68490043 | 89% |
Reaktionsschritte
3-Chloro-N-(1-methyl-1-phenylethyl)benzamide (7.00 g, 25.6 mmol) was dissolved in THF (280 mL), and the solution was added with TMEDA (12.4 mL, 81.9 mmol), then added with sec-butyllithium-hexane solution (0.99 mol/L, 82.7 mL, 81.9 mmol) by drops at −78° C. for 40 minutes under argon atmosphere, followed by stirring at the same temperature for 2.5 hours. Then, the mixture was added with DMF (4.36 mL, 56.3 mmol) and warmed from −78° C. to room temperature over 2 hours. The reaction mixture was added with water, extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by slurry using diisopropyl ether to obtain 4-chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone (6.86 g, yield 89%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07745641B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-f45e4ddcaba84c37bb2475ecd5f8e92f |
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| Quellennotiz | uspto-grants-2010_06 |
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