HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484996Generated: November 2, 2026
Triisopropyl borate → 3-Vinylbenzo[c][1,2]oxaborol-1(3H)-ol
https://huagongshe.com/reaction/1484996
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(2-Bromophenyl)prop-2-en-1-ol | HCID 19102220 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Vinylbenzo[c][1,2]oxaborol-1(3H)-ol | HCID 58169544 | 58.5% |
Reaction Steps
To a suspension of NaH (1.23 g, 28.2 mmol, 1.2 equiv., 60% content) in THF (10 mL) was added a solution of 1-(2-bromophenyl)prop-2-en-1-ol (5.0 g, 23.5 mmol, 1.0 eq) in THF (10 mL) dropwise at 0° C. The mixture was stirred for 1 h, then, cooled to −70° C. n-BuLi (11.3 mL, 28.2 mmol, 1.2 eq., 2.5M in THF) was added. The mixture was stirred for 1 h, then, triisopropyl borate (5.3 g, 28.2 mmol, 1.2 equiv.) was added. The mixture was stirred for 5 h, then, quenched with 2N H2SO4. The mixture was partitioned between brine and ethylacetate. The organic layer was washed over brine, dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography to yield 3-vinylbenzo[c][1,2]oxaborol-1(3H)-ol (2.2 g, 57%). LC-MS (m/z)=158.9, 160.9 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422271B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-c5e79669d2a046c79f107be3e1aa4d28 |
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| Source note | uspto-grants-2016_08 |
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