HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325192Generated: October 30, 2026
Hexane → 4-(Methylthio)phenylboronic acid
https://huagongshe.com/reaction/325192
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | 4-Bromothioanisole | HCID 66037 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Methylthio)phenylboronic acid | HCID 2733959 | 75% |
Reaction Steps
n-BuLi in hexane (2.5M, 625 mmol, 250 ml) is added slowly to a mechanically stirred solution of 4-bromothioanisole (100 g, 492 mmol) in THF (1 ) below −55° C. (internal temp.). After aging at −72° C. for 1 h trimethylborate (73 ml, 1.3 eq.) is added at such a rate to keep the internal temperature below −55° C. After 0.25 h at −78° C. the solution was allowed to warm to 0° C. for 10 min. 2N HCL (500 ml) is added and the solvent is evaporated. Water (500 ml) is added and the product is extracted with EtOAc (1.5 ). The organic layer is dried over Na2SO4, concentrated and the solid is stirred in hexane (500 ml) for 2 h. Filtartion gave 61.9 g (75%) of the desired product. 1H NMR (acetone-d6, 400 MHz) δ7.80 (d, 2H), 7.22 (d, 2H), 7.15 (s, 2H), 2.50 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06222048B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-c8506543b5e145caaa3e13cf5a6602b8 |
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| Source note | uspto-grants-2001_04 |
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