HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 894611Erstellt: 24. Oktober 2026
Potassium Carbonate → alpha-[(5-Acetylamino-4-chloro-2-methoxycarbonylphenyl)oxy]-gamma-butyrolactone
https://huagongshe.com/de/reaction/894611
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2(3H)-Furanone, 3-bromodihydro- | HCID 95463 | — |
| Edukt | Methyl 4-acetamido-5-chloro-2-hydroxybenzoate | HCID 13329485 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | alpha-[(5-Acetylamino-4-chloro-2-methoxycarbonylphenyl)oxy]-gamma-butyrolactone | HCID 12925954 | — |
Reaktionsschritte
51 g. of Methyl 4-acetylamino-5-chloro-2-hydroxybenzoate and 36.8 g. of anhydrous potassium carbonate were suspended in 350 ml. of N,N-dimethylformamide. To the suspension was added 55 g. of α-bromo-γ-butyrolactone, and the mixture was stirred at 60° C. for 12 hours. The solvent was evaporated off under reduced pressure. The residue was diluted with water and extracted with ethyl acetate. The extract was washed with water, dried and concentrated to remove the solvent. The residue was dissolved in chloroform, and subjected to column chromatography on silica gel, using chloroform as the eluent. The product was recrystallized from methanol. By the above procedure there was obtained α-[(5-acetylamino-4-chloro-2-methoxycarbonylphenyl)oxy]-γ-butyrolactone as pale yellow prisms, m.p. 118°-119° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04284644 |
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| Quelldatensatz | uspto-grants-1981_08 |
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| ORD ID | ord-12974d29ce31466e91d9eb068bf367af |
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| Quellennotiz | uspto-grants-1981_08 |
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