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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 3-Bromo-1-(triisopropylsilyl)pyrrole | HCID 2763302 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Triisopropylsilyl)pyrrole-3-boronic acid | HCID 2763303 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07371767B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-ed39a80758d44980a7f8bada2feeb005 |
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| Source note | uspto-grants-2008_05 |
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