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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 41640Erstellt: 24. Oktober 2026

Methanol → Methyl 3-bromothiophene-2-carboxylate

https://huagongshe.com/de/reaction/41640

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktThionyl ChlorideHCID 24386—
Edukt3-Bromothiophene-2-carboxylic acidHCID 2739688—
ProduktMethyl 3-bromothiophene-2-carboxylateHCID 2740074—

Reaktionsschritte

3-Bromothiophene-2-carboxylic acid (5.0 g, 24 mmol, 1 eq.) was dissolved in MeOH (100 mL) and the mixture was degassed and purged with nitrogen (2×). SOCl2 (15 mL, 0.2 mol, 8.3 eq.) was added dropwise and the resulting mixture was stirred overnight at room temperature. The mixture was then concentrated and DCM (150 mL) was added. Saturated NaHCO3 (20 mL) was added, and the resulting mixture was stirred at room temperature for 15 minutes. The organic layer was washed with saturated NaHCO3 (20 mL), water (20 mL), and saturated aqueous NaCl (20 mL), then dried over Na2SO4, filtered and concentrated to yield 3-bromothiophene-2-carboxylic acid methyl ester (4.0 g) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530663B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-80167fa325ac4c73b8b6b32d36edcb90
Quellennotizuspto-grants-2013_09