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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458206Generated: November 2, 2026

Hydrochloric Acid → 2-Cyano-phenylboric acid

https://huagongshe.com/reaction/1458206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
Reactant2-BromobenzonitrileHCID 16272—
ReactantHCID 178418306HCID 178418306—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
Product2-Cyano-phenylboric acidHCID 2170808955.7%

Reaction Conditions

Temperature-76 °C

Reaction Steps

12.4 ml of a 1.6M 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 mmol) 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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849912
Source datasetuspto-grants-1998_12
ORD IDord-15bfbefa11c64c289c937f3e0973d147
Source noteuspto-grants-1998_12