HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422054Generated: November 4, 2026
Triethyl borate → HCID 43145275, compound
https://huagongshe.com/reaction/422054
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethyl borate | HCID 9009 | — |
| Reactant | 1-Bromo-2-(3-methylbutoxy)benzene | HCID 28369546 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 43145275 | HCID 43145275 | 77% |
Reaction Steps
To a solution of 1-bromo-2-(isopentyloxy)benzene (9.68 g, 40 mmol) in THF (160 mL) was added dropwise n-butyl lithium (1.6 M in hexanes, 1.05 eq., 26.3 mL) under nitrogen at −78° C. over 30 min. After further stirring for 1 hour at −78° C., triethylborate (5.86 mL, 51.3 mmol) was added. The cooling bath was removed and the reaction mixture was stirred overnight at rt. An aqueous solution of 2 N HCl (20 mL) was added and the reaction solution stirred for 30 min, at which point 50 mL of water was added. The reaction mixture was extracted with ether (5×80 mL), dried over anhydrous sodium sulfate, filtrated and concentrated to yield 2-(isopentyloxy)phenylboronic acid (6.30 g, 77% yield). 1H NMR (400 MHz, CDCl3): 7.83 (d, 1H), 7.43 (dd, 1H), 7.03 (t, 1H), 6.93 (d, 1H), 6.05 (s, 2H), 4.10 (t, 2H), 1.86-1.75 (m, 3H), 1.0 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101625B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-e00b2e438344430ca8e40a043c88bccb |
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| Source note | uspto-grants-2012_01 |
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