Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 7-Bromobenzo[b]thiophene | HCID 12045538 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Benzothien-7-ylboronic acid | HCID 16640528 | 60% |
Reaction Steps
A solution of 7-bromo-1-benzothiophene (19.9 g, 0.094 mol) in absolute ether (200 ml) was treated with a 1.6 M solution of n-butyllithium in hexane (0.14 mol, 88 ml) at −78° C. The solution was stiffed at −78° C. for 10 minutes then treated with trimethyl borate (15 ml, 0.14 mol). The mixture was allowed to warm to −10° C. then quenched with an excess of dilute hydrochloric acid. The organic layer was separated, dried, evaporated, and the residue was recrystallised from aqueous ethanol to yield the title compound (10 g, 60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442701B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-ece564e6cbef422489e0a200676991f5 |
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| Source note | uspto-grants-2008_10 |
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