HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422364Generated: October 31, 2026
Tributyl borate → (2-ethyl-4-methoxyphenyl)boronic acid
https://huagongshe.com/reaction/2422364
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributyl borate | HCID 12712 | — |
| Reactant | 1-BROMO-2-ETHYL-4-METHOXY-BENZENE | HCID 12386619 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-ethyl-4-methoxyphenyl)boronic acid | HCID 11506554 | — |
Reaction Steps
A solution of 4-bromo-3-ethyl anisole (94 g, 0.437 mol) in THF (900 ml) was cooled to −78° C. n-Butyl lithium (249 ml, 0.55 mol) was added dropwise at the same temperature. Stirring was continued for 1 hr at −78° C. Tri-n-butyl borate (177 ml, 0.655 mol) was added slowly at −78° C. The cooling bath was removed, the reaction mixture was allowed to warm to 0° C. and was quenched with 1.5 N hydrochloric acid at 0° C. The organic layer was separated. The aqueous layer was extracted with ethylacetate and the combined organic layers were washed with brine and concentrated. The residue obtained was stirred in petroleum ether for 30 min. The solid obtained was filtered and dried under vacuum. Yield: 65 g, 82%, as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960349B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-79297b6526e8447bbf326fd1a6530edc |
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| Source note | uspto-grants-2011_06 |
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