HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1977350Erstellt: 25. Oktober 2026
Allyl bromide → 3-Allyloxycarbonyl-5-nitrobenzoic acid
https://huagongshe.com/reaction/1977350
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Allyl bromide | HCID 7841 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 5-Nitroisophthalic acid | HCID 12069 | — |
| Edukt | 4-Acetylthio-1-(4-nitrobenzyloxycarbonyl)-2-carboxypyrrolidine | HCID 13504324 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 3-Allyloxycarbonyl-5-nitrobenzoic acid | HCID 20655860 | — |
| Produkt | 3-amino-5(N-methyl-methoxycarbamoyl)-benzoic acid allyl ester | HCID 22986142 | — |
Reaktionsschritte
Starting material (1(c)) was prepared as described in Example 1. Starting material 7(d) was prepared as follows. A mixture of potassium carbonate (17.00 g), 5-nitroisophthalic acid (52.00 g), allyl bromide and dimethylacetamide (400 ml) was stirred at 90° for 4 h. Dimethylacetamide was evaporated away under reduced pressure and the residue was dissolved in ethyl acetate. washed with water (2×300 ml) and then extracted with aqueous saturated sodium bicarbonate solution (3×300 ml). The extracts were combined. acidified to pH 4 with concentrated hydrochloric acid and reextracted with ethyl acetate (2×300 ml). The extracts were combined, washed with water (300 ml), dried over magnesium sulphate and evaporated under reduced pressure to give 5-nitro-isophthalic acid 3-allyl ester (7(a)) as a cream solid (39.48 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06232338B1 |
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| Quelldatensatz | uspto-grants-2001_05 |
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| ORD ID | ord-5c07b5f909e54b85831969a35cf2c882 |
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| Quellennotiz | uspto-grants-2001_05 |
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