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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 746825Erstellt: 26. Oktober 2026

Methanol → 1-(Triisopropylsilyl)pyrrole-3-boronic acid

https://huagongshe.com/reaction/746825

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktTrimethyl borateHCID 8470—
Edukt3-Bromo-1-(triisopropylsilyl)pyrroleHCID 2763302—
EduktHCID 178418306HCID 178418306—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(Triisopropylsilyl)pyrrole-3-boronic acidHCID 2763303—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To −78° C. solution of 3-bromo-1-(triisopropylsilyl)-1H-pyrrole (0.619 g, 2.288 mmol) in 10 mL THF was added tert-butyllithium (2.83 mL of 1.7 M in Heptane, 4.80 mmol) dropwise. The reaction mixture was stirring at −78° C. for 45 minutes, then trimethylborate (2.38 g, 22.88 mmol) was added. The reaction was stirred for another 45 minutes at −78° C. To this was then added 0.9 mL methanol and water solution (V/V=1:1) and the reaction was allowed warm to room temperature. The reaction mixture was quenched with H2O (30 mL), then extracted with EtOAc (3×30 mL) and the combined organic extracts washed with brine. The organic phase was dried over Na2SO4 and concentrated in vacuo, and used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07393959B2
Quelldatensatzuspto-grants-2008_07
ORD IDord-f3c9ff7386824966b7599ee99336e74b
Quellennotizuspto-grants-2008_07