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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1853909Generated: October 25, 2026

1,3-Diiodopropane → 1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutanecarbonitrile

https://huagongshe.com/reaction/1853909

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DiiodopropaneHCID 12314—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
Reactant2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetonitrileHCID 3842922—
SolventTetrahydrofuranHCID 8028—
Product1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclobutanecarbonitrileHCID 5803466348.7%

Reaction Steps

To a solution of 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetonitrile (7.0 g, 29 mmol) in THF at 0° C. was added NaHMDS (1.0 M, 120 mL, 120 mmol). After stirring for 20 min 1,3-diiodopropane (26 g, 86 mmol) was added and the reaction mixture was stirred at room temperature for 2 h. The reaction mixture was cooled to 0° C., quenched with MeOH (5.0 mL) and the residue was purified by column chromatography (silica, ethyl acetate/hexanes gradient) to afford the desired product (4.0 g, 47%) as a yellow oil: ESI MS m/z 286 [C17H22BNO2+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962648B2
Source datasetuspto-grants-2015_02
ORD IDord-50a100c791c649b49232818f576ab13a
Source noteuspto-grants-2015_02