HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732775Generated: October 30, 2026
Hydrochloric Acid → 2-Methyl-4-methylthiophenylboronic acid
https://huagongshe.com/reaction/732775
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | (4-Bromo-3-methylphenyl)(methyl)sulfane | HCID 26370189 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Methyl-4-methylthiophenylboronic acid | HCID 22591298 | 52.4% |
Reaction Steps
Add 1-bromo-2-methyl-4-methylsulfanyl-benzene (608 mg, 2.80 mmol) to diethyl ether (60 mL) and cool to −78° C. under a nitrogen blanket. Add t-BuLi (3.4 mL, 5.78 mmol) over a 15 minute period, stir for 2 minutes, add trimethyl borate ((MeO)3B, 340 μL, 2.99 mmol) over 2 minutes, stir for 15 minutes at −78° C. and then let warm to room temperature. Quench the reaction with saturated aqueous NH4Cl (7 mL), stir for 15 minutes, add 1M aqueous HCl (6 mL), stir for another 2 minutes and separate. Dry with Na2SO4, filter (wash the drying agent with ethyl acetate (3×20 mL)), and concentrate. Chromatograph the crude material on a SiO2 column with 20% ethyl acetate in hexanes to 5% methanol in ethyl acetate to give 267 mg of the title compound (52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07585977B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-4aa0e0162f9a4a2096032d1eb077458b |
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| Source note | uspto-grants-2009_09 |
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