HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15268Erstellt: 26. Oktober 2026
Water → 5-Fluoro-1-(4-methoxybenzyl)indoline-2,3-dione
https://huagongshe.com/reaction/15268
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Edukt | 5-Fluoroisatin | HCID 236566 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl acetate hexane | HCID 21226206 | — |
| Produkt | 5-Fluoro-1-(4-methoxybenzyl)indoline-2,3-dione | HCID 7677100 | 80% |
Reaktionsschritte
5-Fluoro-1H-indole-2,3-dione (956 mg, 5.79 mmol, 1 eq) was added as a solution in dry DMF to a stirred slurry of sodium hydride (278 mg, 11.6 mmol, 2 eq) in dry DMF drop wise over 15 minutes under an inert atmosphere with adequate pressure release to accommodate H2 evolution. The resulting mixture was stirred for 1 hour and p-methoxybenzyl chloride was added via syringe to the reaction. The solution was then stirred ca 2 hours and worked up by addition of water followed by extraction into ethyl acetate. The organic layer was washed twice with water and then dried over MgSO4. Column chromatography with ethyl acetate/hexane afforded 5-Fluoro-1-(4-methoxy-benzyl)-1H-indole-2,3-dione as a red solid (1.3 g, 80% yield). 1H NMR (CDCl3) δ (ppm): 7.3-7.24 (m, 3H), 7.20 (td, J=8.7, 2.7 Hz, 1H), 6.9-6.86 (m, 2H), 6.76 (dd, J=8.6, 3.6 Hz, 1H), 3.81 (s, 2H), 3.78 (s, 3H). LC/MS=286.1 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07732449B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-dbc008b6d4344431a0479a5e6a29980f |
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| Quellennotiz | uspto-grants-2010_06 |
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