HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 542583Erstellt: 26. Oktober 2026
Indomethacin → Allyl 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-3-indoleacetoxyacetate
https://huagongshe.com/reaction/542583
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Indomethacin | HCID 3715 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Allyl chloroacetate | HCID 76206 | — |
| Katalysator | Benzyl triethylammonium chloride | HCID 66133 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | Allyl 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-3-indoleacetoxyacetate | HCID 13654465 | — |
Reaktionsschritte
25 g of indometacin, 10 g of potassium carbonate and 1.0 g of benzyltriethylammonium chloride in 140 ml of acetone are stirred for 30 minutes at 50° to 60° C. 10.1 g of allyl chloroacetate are then added dropwise over 5 minutes. The mixture is stirred at 40° C. until the reaction has ended (as checked by thin layer chromatography; about 3 hours). The mixture is filtered while warm, the filtrate is evaporated in vacuo and the residue is taken up in ether (about 90 ml) and mixed with petroleum ether (40 to 60) (about 30 ml). This mixture is left to stand over night at -10° C. and the product is then filtered off and dried in vacuo.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04658039 |
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| Quelldatensatz | uspto-grants-1987_04 |
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| ORD ID | ord-3b0c8e80d6994da7b2c54c4961999ab1 |
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| Quellennotiz | uspto-grants-1987_04 |
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