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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 502858Erstellt: 26. Oktober 2026

Hydrochloric Acid → (4-(1-Hydroxycyclopropyl)phenyl)boronic acid

https://huagongshe.com/reaction/502858

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktMethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoateHCID 2773500—
EduktHCID 178418443HCID 178418443—
KatalysatorTitanium isopropoxideHCID 11026—
LösungsmittelDiethyl EtherHCID 3283—
Produkt(4-(1-Hydroxycyclopropyl)phenyl)boronic acidHCID 57416393—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A 3.0 M solution of ethylmagnesium bromide in diethylether (7.6 mL) is added to a stirred solution of titanium(IV) isopropoxide (2.2 mL) in diethylether (70 mL) chilled to −78° C. The resultant solution is stirred at −78° C. for 1.5 h, before 4-(4,4,5,5-tetramethyl-[1,3,2]dioxa borolan-2-yl)-benzoic acid methyl ester (2.0 g) is added. The reaction mixture is warmed to ambient temperature and stirred for an additional 12 h. Then, 1 M aqueous hydrochloric acid is added and the resulting mixture is extracted with ethyl acetate. The combined organic extracts are dried (sodium sulphate) and the solvent is evaporated. The residue is dissolved in acetone (60 mL) and 0.1 M aqueous NH4OAc solution (50 mL) followed by NalO4 (2.3 g) is added. The resulting reaction mixture is stirred at room temperature for 18 h. After removal of the acetone, the residue is extracted with ethyl acetate. The combined extracts are dried (sodium sulphate) and the solvent is evaporated. The residue is purified by chromatography on silicagel (cyclohexane/ethyl acetate).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07776830B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-c056499d41ec42609bb9c55e3547a795
Quellennotizuspto-grants-2010_08