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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37517Erstellt: 23. Oktober 2026

Trimethyl borate → 4-(Methylthio)phenylboronic acid

https://huagongshe.com/de/reaction/37517

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethyl borateHCID 8470—
EduktSodium HydroxideHCID 14798—
Edukt4-BromothioanisoleHCID 66037—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt4-(Methylthio)phenylboronic acidHCID 273395983,3%

Reaktionsschritte

Under nitrogen, a stirred solution of 30 g (150 mmol) of 4-bromothioanisole (Aldrich) in 1500 mL of anhydrous THF at -78 ° C. was treated with 180 mmol of n-butyllithium in hexane. After 30 minutes, 51 mL (450 mmol) of trimethylborate was added neat and the reaction was allowed to warm to ambient temperature overnight. A solution of 300 mL of 10% NaOH was added and the mixture stirred vigorously for lb. The solvent was removed in vacuo, the pH adjusted to 4-5, and the product collected by filtration. Repeated washings with hexane and water provided 21 g (83%) of 4-methylthiophenylboronic acid (21 in Synthetic Scheme VII when R5 =SCH3 and R3, R4, R6, and R7 =H) as a colorless solid: NMR (DMSO-d6) d 2.47 (s, 3H), 7.20 (d, J=8 Hz, 2H), 7.71 (d, J=8 Hz, 2H), 7.96 (br s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05420287
Quelldatensatzuspto-grants-1995_05
ORD IDord-2b95209fadce47fba1a904e47c6976a4
Quellennotizuspto-grants-1995_05