HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640639Generated: October 29, 2026
Triisopropyl borate → HCID 57356028, compound
https://huagongshe.com/reaction/1640639
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | HCID 59133208 | HCID 59133208 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 57356028 | HCID 57356028 | — |
Reaction Steps
To a solution of 7-trifluoromethyl-benzo[b]thiophene (0.52 g, 0.0026 mol) in THF (30 mL) at −78° C. was added 2.5 M of n-BuLi in hexane (1.4 mL). The reaction was then slowly warmed up to −30° C. over 30 min. and stirred at this temperature for 10 min prior to recooling to −78° C. and treatment with triisopropyl borate (0.7255 g, 0.0038 mol). The reaction was then slowly warmed up to 0° C. then was quenched with saturated ammonium chloride and the solvent removed in vacuo. To the residue was added aqueous sodium hydroxide (10 mL, 2N solution) followed by water (30 mL) then this mixture was extracted with DCM. The aqueous solution was acidified using dilute sulfuric acid (2N solution), filtered and the residue dried in vacuo to yield 7-trifluoromethylbenzo[b]thiophen-2-boronic acid. 1H NMR (400 MHz, MeOD) δ ppm 7.55 (1 H, t, J=7.45 Hz), 7.75 (1 H, d, J=7.07 Hz), 8.02 (1 H, s) and 8.17 (1 H, d, J=7.83 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08114846B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-69bf280ee31040f89b76eb8bcb4dd37f |
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| Source note | uspto-grants-2012_02 |
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