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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034433Generated: October 30, 2026

N,N,N',N'-Tetramethylethylenediamine → (5-Methyl-1-benzofuran-2-yl)boronic acid

https://huagongshe.com/reaction/1034433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantTriisopropyl borateHCID 21531—
Reactant5-MethylbenzofuranHCID 33103—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product(5-Methyl-1-benzofuran-2-yl)boronic acidHCID 15680843—

Reaction Conditions

Temperature-10 °C

Reaction Steps

n-Butyl lithium (1.7M, 35.16 ml) was added dropwise to a stirred solution of TMEDA (9.58 ml) and 5-methylbenzofuran (8.22 g) in ether (250 ml) maintaining the temperature below -60° C. throughout. The solution was warmed to about -10° C. over 45 minutes and stirred at this temperature for 30 minutes. A precipitate formed on warming. The suspension was cooled and triisopropylborate (43 ml) was added, maintaining the temperature below -60° C. The solution was warmed gradually to room temperature before quenching with 2N HCl (70 ml). The mixture was extracted with ether (3×50 ml) and the combined organic extracts washed with 2N HCl (4×30 ml), water (2×30 ml) and dried before evaporation to give the title compound as an orange solid (12.75 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05317023
Source datasetuspto-grants-1994_05
ORD IDord-9c7beb916dcd426199346144dd3081f8
Source noteuspto-grants-1994_05