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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 357739Erstellt: 23. Oktober 2026

Methyl 3-bromothiophene-2-carboxylate → 3-Bromothiophene-2-carboxylic acid

https://huagongshe.com/de/reaction/357739

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 3-bromothiophene-2-carboxylateHCID 2740074—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelSodium HydroxideHCID 14798—
Produkt3-Bromothiophene-2-carboxylic acidHCID 273968897,3%

Reaktionsschritte

3-Bromo-2-thiophenecarboxylic acid methyl ester (7.74 g) was dissolved in a mixture of methanol (35 ml) and tetrahydrofuran (35 ml), and 1N aqueous sodium hydroxide (53 ml) was added. The mixture was stirred at room temperature for 2 hours and washed with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 3-bromo-2-thiophenecarboxylic acid (7.05 g) as crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05840917
Quelldatensatzuspto-grants-1998_11
ORD IDord-2e768a02cf3442ff911f2d68e5377a5c
Quellennotizuspto-grants-1998_11