HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1611491Erstellt: 25. Oktober 2026
Nitric Acid → 4-(5-Nitro-thiophen-2-yl)-butyric acid methyl ester
https://huagongshe.com/reaction/1611491
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Nitric Acid | HCID 944 | — |
| Edukt | 4-(2-Thienyl)butanoic acid methyl ester | HCID 140766 | — |
| Lösungsmittel | Acetic Anhydride | HCID 7918 | — |
| Produkt | 4-(5-Nitro-thiophen-2-yl)-butyric acid methyl ester | HCID 69233400 | — |
Reaktionsschritte
To 8 mL of acetic anhydride at −20° C. is added 1.2 mL of nitric acid (d=1.5). The mixture is kept at −20° C., and a solution of 4-thiophen-2-yl-butyric acid methyl ester (1.84 g, 10.0 mmol) in 12 mL of acetic anhydride is added dropwise. The reaction mixture is stirred for 10 minutes after completion of addition, and poured into an ice-water mixture. The product is extracted with ethyl acetate and the organic layer is washed with 10 N aqueous sodium hydroxide solution, dried and concentrated. The residue is purified by flash column chromatography eluting with 1:4 ethyl acetate:hexane to provide 1.32 g of 4-(5-nitro-thiophen-2-yl)-butyric acid methyl ester as a yellow oil; 1H NMR (DMSO-d6) δ 1.93 (quintet, J=7 Hz, 2H), 2.41 (t, J=7 Hz, 2H), 2.88 (t, J=7 Hz, 2H), 3.59 (s, 3H), 7.04 (d, J=5 Hz, 1H), 8.01 (d, J=5 Hz, 1H); MS 229.0 (M)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06987116B2 |
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| Quelldatensatz | uspto-grants-2006_01 |
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| ORD ID | ord-428f1f5596d141b0bd4ef094d4044da1 |
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| Quellennotiz | uspto-grants-2006_01 |
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