HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604224Generated: November 2, 2026
Trimethyl borate → 5-Sec-butyl-1-methoxy-benzene boronic acid
https://huagongshe.com/reaction/604224
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Bromo-1-methoxy-4-(1-methylpropyl)benzene | HCID 66602978 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Sec-butyl-1-methoxy-benzene boronic acid | HCID 86626524 | — |
Reaction Steps
2-Bromo-4-sec-butyl-1-methoxy-benzene (1.15 g) is dissolved in tetrahydrofuran (17 ml) and the mixture is cooled to −78° C., and thereto is added dropwise 1.6M n-butyllithium in hexanes, and the mixture is stirred at −78° C. for 15 minutes. To the reaction solution is added trimethyl borate (1.47 g), and the reaction mixture is stirred at −78° C. for 30 minutes, and thereto are added a saturated aqueous ammonium chloride solution and ethyl acetate. The mixture is separated, and the organic layer is washed with a saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give crude 5-sec-butyl-1-methoxy-benzene boronic acid (950 mg). NMR (CDCl3): 0.81 (3H, t), 1.22 (3H, d), 1.58 (2H, m), 2.58 (1H, m), 3.90 (3H, s), 6.25 (2H, s), 6.85 (2H, d), 7.25 (1H, d), 7.65 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906517B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-41d7710d29104a60b03e11c7c459f28a |
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| Source note | uspto-grants-2011_03 |
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