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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222272Generated: October 31, 2026

Methanol → 1-(Triisopropylsilyl)pyrrole-3-boronic acid

https://huagongshe.com/reaction/2222272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTrimethyl borateHCID 8470—
Reactant3-Bromo-1-(triisopropylsilyl)pyrroleHCID 2763302—
ReactantHCID 178418306HCID 178418306—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(Triisopropylsilyl)pyrrole-3-boronic acidHCID 2763303—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 3-bromo-1-(triisopropylsilyl)-1H-pyrrole (0.691 g, 2.28 mmol) in THF (10 mL) at −78° C. was added t-butyllithium (2.83 mL, 4.80 mmol of 1.7M solution in heptane). The solution was stirred at −78° C. for 45 min, then trimethylborate (2.38 g, 22.8 mmol) was added and stirred at −78° C. for 20 min. The reaction mixture was allowed to warm to rt and then cooled again to −78° C. before methanol:water (V:V=1:1, 0.9 mL) was added and the solution allowed warm to rt. The reaction mixture was quenched with brine (10 mL) and extracted with EtOAc (3×25 mL). The combined organic phase was washed with brine, dried over Na2SO4 and concentrated in vacuo to give crude 1-(triisopropylsilyl)-1H-pyrrol-3-ylboronic acid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371767B2
Source datasetuspto-grants-2008_05
ORD IDord-ed39a80758d44980a7f8bada2feeb005
Source noteuspto-grants-2008_05