HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854169Generated: October 26, 2026
Hexane → (5-(Tert-butyl)-2-((2-methoxyethoxy)methoxy)phenyl)boronic acid
https://huagongshe.com/reaction/1854169
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 2-Bromo-4-(tert-butyl)-1-((2-methoxyethoxy)methoxy)benzene | HCID 86718561 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-(Tert-butyl)-2-((2-methoxyethoxy)methoxy)phenyl)boronic acid | HCID 86718562 | 98% |
Reaction Steps
n-Butyllithium in hexane (2.5 M, 4.2 mL, 10.5 mmol) was added dropwise to a solution of give 2-bromo-4-(tert-butyl)-1-((2-methoxyethoxy)methoxy)benzene (3.0 g, 9.46 mmol) and trimethyl borate (1.2 mL, 10.76 mmol) in anhydrous tetrahydrofuran (20 mL) at −78° C. under nitrogen. The reaction mixture was stirred at −78° C. for 20 minutes then at 0° C. for an additional 20 minutes. The reaction was then quenched by the addition of water (20 mL) and the mixture extracted with ether (100 mL). The organic layer was separated, dried (MgSO4), filtered and concentrated under reduced pressure to give (5-(tert-butyl)-2-((2-methoxyethoxy)methoxy)phenyl)boronic acid (2.61 g, 98% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962657B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-10aaf23982e64ff9b246c09063ffbe67 |
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| Source note | uspto-grants-2015_02 |
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