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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1178617Erstellt: 26. Oktober 2026

Nitric Acid → 4-(5-Nitro-thiophen-2-yl)-butyric acid methyl ester

https://huagongshe.com/reaction/1178617

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitric AcidHCID 944—
Edukt4-(2-Thienyl)butanoic acid methyl esterHCID 140766—
LösungsmittelAcetic AnhydrideHCID 7918—
Produkt4-(5-Nitro-thiophen-2-yl)-butyric acid methyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07276519B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-ce786d9bf66a402ab74423ada59df1fb
Quellennotizuspto-grants-2007_10