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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 651399Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2-Cyano-phenylboric acid

https://huagongshe.com/reaction/651399

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTrimethyl borateHCID 8470—
Edukt2-BromobenzonitrileHCID 16272—
EduktHCID 178418306HCID 178418306—
LösungsmittelPentaneHCID 8003—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Cyano-phenylboric acidHCID 2170808955,7%

Reaktionsbedingungen

Temperatur-76 °C

Reaktionsschritte

12.4 ml of a 1.6 M solution of t-butyllithium in n-pentane was dropwise added to 23 ml of THF at −76° C. in about 10 minutes. Then, a solution of 2.0 g (11.0 mmo ) of 2-bromobenzonitrile in 3.0 ml. of THF was dropwise added to the resulting mixture at −76° C. in about 20 minutes, followed by the dropwise addition of 2.3 ml (19.8 mmol) of trimethoxyborane in 7 minutes. The obtained mixture was stirred at −76° C. for 20 minutes, followed by the addition of 13.8 ml of 2N hydrochloric acid. The obtained mixture was stirred at room temperature for 30 minutes and extracted with ethyl acetate. The ethyl acetate phase was washed with water and a saturated brine, dried and distilled to remove the solvent. 15 ml of methylene chloride and 15 ml of n-hexane were added to the obtained residue. The obtained mixture was stirred at room temperature for 30 minutes to give a precipitate. The precipitate was recovered by filtration and dried to give 0.9 g of the title compound (yield: 55.7%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06281214B1
Quelldatensatzuspto-grants-2001_08
ORD IDord-44b71ad8881b4693a285acf43cbc0a64
Quellennotizuspto-grants-2001_08