HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1169450Erstellt: 27. Oktober 2026
Dimethylformamide → Methyl 7-[(2-chlorobenzyl)oxy]-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxylate
https://huagongshe.com/reaction/1169450
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2-Chlorobenzyl chloride | HCID 11906 | — |
| Edukt | Methyl 7-hydroxy-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxylate | HCID 22989977 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Methyl 7-[(2-chlorobenzyl)oxy]-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxylate | HCID 22990149 | — |
Reaktionsschritte
A mixture of methyl 7-hydroxy-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxylate (400 mg), 2-chlorobenzyl chloride (0.25 ml), potassium carbonate (309 mg) and DMF (10 ml) was stirred at 60° C. for 5 hours. The reaction mixture was mixed with water and was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated solution of sodium chloride and was dried with magnesium sulfate. After concentration under reduced pressure, the residue was subjected to separation and purification using column chromatography (ethyl acetate/hexane 1:2) to obtain methyl 7-[(2-chlorobenzyl)oxy]-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxylate (413 mg) as colorless crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06627651B1 |
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| Quelldatensatz | uspto-grants-2003_09 |
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| ORD ID | ord-67ed8b6796ab4a1588dede16d66614cc |
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| Quellennotiz | uspto-grants-2003_09 |
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