HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496791Generated: October 29, 2026
Hydrochloric Acid → (2-Ethylthiophenyl)boronic acid
https://huagongshe.com/reaction/496791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Triisopropyl borate | HCID 21531 | — |
| Reactant | 1-Bromo-2-(ethylsulfanyl)benzene | HCID 13082725 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (2-Ethylthiophenyl)boronic acid | HCID 3785655 | — |
Reaction Steps
9.5 g (50 mmol) of triisopropyl borate are added to a solution of 10.9 g (50.0 mmol) of 1-bromo-2-ethylsulfanylbenzene kept at −70° C. 33.3 ml of a 15% solution of BuLi in hexane (55 mmol) are then added. The mixture is stirred at −70° C. for a further 30 minutes, then 1 N hydrochloric acid and ethyl acetate are added. The organic phase is separated off, dried and evaporated. The residue is taken up in diethyl ether and filtered. A colourless solid is obtained; FAB 182
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06946489B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-8215473de7e84f9db4a581d52f40e108 |
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| Source note | uspto-grants-2005_09 |
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