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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403483Generated: October 30, 2026

2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → HCID 70665171, compound

https://huagongshe.com/reaction/1403483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5017741—
Reactant2-(4-Fluorophenyl)furanHCID 11615223—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70665171HCID 70665171—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2-(4-fluorophenyl)furan (1.50 g, 9.25 mmol) in dry tetrahydrofuran (100 mL) was added a solution of n-BuLi (4.4 mL, 2.5M solution in hexane) dropwise with stirring at −78° C. under nitrogen. The resulting solution was warmed slowly to −40° C. over 45 min and stirred at this temperature for another 30 min. The mixture was cooled again below −78° C. followed by dropwise addition of 4,4,5,5-tetramethyl-2-(propan-2-yloxy)-1,3,2-dioxaborolane (3.42 g, 18.38 mmol). After warming to room temperature, the mixture was quenched with NH4Cl (aq) and extracted with ethyl acetate (3×80 mL). The combined organic layers were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the residue (1.20 g crude), which was used to the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912188B2
Source datasetuspto-grants-2014_12
ORD IDord-4f3ac8b1289a4656ae22bc94302443f4
Source noteuspto-grants-2014_12