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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 629841Erstellt: 26. Oktober 2026

Hydrochloric Acid → 873806-20-3

https://huagongshe.com/reaction/629841

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5017741—
EduktButyllithiumHCID 178418339—
EduktHCID 178462446HCID 178462446—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt873806-20-3HCID 12171955—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a stirred solution of Ia (7.0 g, 50 mmol) in dry THF (25 mL) at −78° C. was added n-BuLi (1.6 M in n-hexane, 62.5 mL, 100 mmol). After being stirred for 1 hour at −78° C., the reaction mixture was warmed to room temperature and stirred for 1 hour at that temperature. Another flask was charged with 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (7.8 mL, 38 mmol) in dry THF (50 mL) under argon atmosphere, and the reaction mixture was cooled to −78° C. The lithium acetylide from the first flask, which was cooled to −78° C., was slowly added to the second by a double-ended needle. The mixture was stirred at −78° C. for 2 hours, after which anhydrous HCl (100 mmol) was added. Then, reaction mixture was warmed to room temperature. After removal of the precipitated LiCl by filtration and removal of solvents under reduced pressure, the residue was purified by distillation (113-115° C./7 mbar) to afford IIIa (5.9 g, 80%) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09315525B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-d0388a5d128947039f58c65e1a47e386
Quellennotizuspto-grants-2016_04