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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 234455Erstellt: 25. Oktober 2026

2-Methylthiophene → (5-Methylthiophen-2-yl)boronic acid

https://huagongshe.com/reaction/234455

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-MethylthiopheneHCID 11126—
EduktTriisopropyl borateHCID 21531—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(5-Methylthiophen-2-yl)boronic acidHCID 273437488,8%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

n-BuLi (2.38M, 16 ml) was slowly added to a solution of 2-methyl thiophene (3.0 g, 31 mmol) in THF (20 ml) at -78° C. The solution was kept at -78° C. for 10 min. then warmed to 0° C. for an additional 0.5 hr. The solution was then transferred by steel canula under nitrogen into a vessel containing triisopropylborate (6.3 g, 33 mmol) in ether (15 ml) at -78° C. The resulting milky white solution was stirred at -78° C. for 20 min. then at room temperature for 2 hours. The reaction was quenched by the addition of 10% aqueous HCl (5.0 ml) and the solution was extracted into ether. The combined ether extracts were extracted with 10M NaOH (2×30 ml), the aqueous extracts were acidified with dilute HCl to pH 2 and extracted into ether (3×25 ml). The combined ether extracts were washed once with water (10 ml), once with brine (10 ml) and dried and evaporated to give 3.91 g 2-methylthiophene-5-boronic acid as a light brown solid. This was used in the next step with no further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05594021
Quelldatensatzuspto-grants-1997_01
ORD IDord-db4164171c3d40ad9a80e9084f9aeea7
Quellennotizuspto-grants-1997_01