HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918324Generated: November 1, 2026
Water → 3-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-benzeneboronic Acid
https://huagongshe.com/reaction/1918324
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | (3-Bromophenethoxy)(tert-butyl)dimethylsilane | HCID 11515183 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 3-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-benzeneboronic Acid | HCID 58845136 | — |
Reaction Steps
50.0 g of [2-(3-bromo-phenyl)-ethoxy]-tert-butyl-dimethyl-silane were dissolved in 500 ml of anhydrous THF. 64.6 ml of a 2.7 M solution of n-butyllithium in n-heptane were added dropwise at −70° C. The mixture was stirred for 1 h at −70° C. Then 40.2 ml of triisopropyl borate were added dropwise at −70° C. Stirring was continued for 30 min at −70° C. and the mixture allowed to warm up to −20° C. 500 ml of water were added and the mixture was extracted three time with 500 ml each of DCM. The combined organic layers were dried with magnesium sulfate and evaporated to yield 43.6 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618304B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-d1149202c59f4c48b871c5c4649e2835 |
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| Source note | uspto-grants-2013_12 |
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