HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942670Generated: November 3, 2026
Triisopropyl borate → {2-(methyloxy)-3-[(E)-2-(methyloxy)ethenyl]phenyl}boronic acid
https://huagongshe.com/reaction/1942670
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 1-bromo-2-(methyloxy)-3-[(E)-2-(methyloxy)ethenyl]benzene | HCID 58494123 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {2-(methyloxy)-3-[(E)-2-(methyloxy)ethenyl]phenyl}boronic acid | HCID 58494144 | — |
Reaction Steps
To a solution of 1-bromo-2-(methyloxy)-3-[(E)-2-(methyloxy)ethenyl]benzene (D100) (930 mg, 3.83 mmol) in Tetrahydrofuran (THF) (10 mL) was added BuLi (1.989 mL, 4.97 mmol) dropwise at −78° C. under nitrogen. The reaction mixture was stirred at −78° C. for 2 hours. Tris(1-methylethyl) borate (1.319 mL, 5.74 mmol) was added to the reaction mixture by syringe at −78° C. Then the reaction was stirred at −78° C. for 30 min, and then warmed to room temperature slowly. Then the reaction was quenched with water. The mixture was extracted with EA (15 mL×3). The combined organic layers was dried over anhydrous sodium sulphate. After filtration and concentration, the crude {2-(methyloxy)-3-[(E)-2-(methyloxy)ethenyl]phenyl}boronic acid (D101) (741 mg) was used directly in the next step. MS (ES): C10H13BO4 requires 208.1. found 209.0 (M+H+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389508B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-7c6bb231cefb4316a39223c4fab26790 |
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| Source note | uspto-grants-2013_03 |
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