HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217207Generated: October 29, 2026
Triisopropyl borate → 5-Ethoxymethoxy-benzofuran-2-boronic acid
https://huagongshe.com/reaction/217207
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 5-Ethoxymethoxy-benzofuran | HCID 59227450 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Ethoxymethoxy-benzofuran-2-boronic acid | HCID 46183970 | 52.2% |
Reaction Steps
To a stirred solution of 5-ethoxymethoxy-benzofuran (3) (265 mg, 1.38 mmol) in THF (5 mL) at −78° C., n-butyllithium (2.5M solution in hexane, 0.56 mL, 1.44 mmol) was added drop wise. After the reaction mixture was stirred for 1 hour, triisopropylborate (0.635 mL, 2.76 mmol) was added slowly and the stirring was continued for additional 20 minutes at −78° C. The reaction mixture was quenched with saturated ammonium chloride solution (10 mL) and was allowed to warm to room temperature. Water (10 mL) was added and the resulting mixture was extracted in diethyl ether (2×50 mL). The combined extracts were washed with brine, dried over MgSO4, and concentrated under reduced pressure. Purification of the crude product by recrystallization from ethyl acetate and hexane afforded the desired compound (4) (170 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193363B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-2165f1b4e5124f308205c5b1fc2cfddb |
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| Source note | uspto-grants-2012_06 |
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