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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920842Generated: November 2, 2026

2-Methoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → 3-Bromo-α,α-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzeneacetonitrile

https://huagongshe.com/reaction/1920842

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 10975759—
ReactantHCID 58366812HCID 58366812—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-α,α-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzeneacetonitrileHCID 5796963395.4%

Reaction Conditions

Temperature-10 °C

Reaction Steps

A solution of isopropylmagnesium chloride lithium chloride complex (1.71 ml, 1.65 mmol) in tetrahydrofuran (10 ml) was cooled down to −20° C. 2-(3,5-dibromophenyl)-2-methylpropanenitrile (500 mg, 1.65 mmol, preparation as described in Example 2 step 1) was added in one portion and the reaction stirred for 1.5 hours at −15 to −5° C. 2-Methoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (260.7 mg, 269.9 μL, 1.65 mmol) was added and the reaction was allowed to warm up to room temperature. The reaction mixture was stirred at room temperature for 18 hours. The mixture was partitioned between a diluted solution of ammonium chloride and ethyl acetate. The organic phase was dried over magnesium sulfate and the solvent removed under reduced pressure to afford the title compound as a light yellow solid (551 mg, 95% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173635B2
Source datasetuspto-grants-2012_05
ORD IDord-3cc6e63aa41f4fd6ab1d8fb963feb81e
Source noteuspto-grants-2012_05