HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007466Generated: October 30, 2026
Sulfuric Acid → (4-Methoxyphenyl)boronic acid
https://huagongshe.com/reaction/1007466
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Bromoanisole | HCID 7730 | — |
| Reactant | Triethyl borate | HCID 9009 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (4-Methoxyphenyl)boronic acid | HCID 201262 | — |
Reaction Steps
100 ml of a solution of 10 g of p-bromoanisole in anhydrous diethyl ether is added dropwise under reflux to a suspension, under inert gas, of 1.3 g of magnesium turnings in 5 ml of anhydrous diethyl ether, and the mixture is left under reflux for 2 hours. The reaction medium is then poured into a solution of 9.02 ml of triethylborate in 60 ml of anhydrous ether cooled down to −70° C. After agitation for 1 hour at −70° C., then for 1 hour at ambient temperature, the solution is poured into a mixture comprising 11 ml of sulphuric acid and 50 g of ice and water followed by agitation for 1 hour. The organic phase is extracted with 100 ml of an aqueous solution saturated in sodium bicarbonate, the aqueous phases are combined, then reacidified with 6N hydrochloric acid, extracted with ether, dried and evaporated under reduced pressure. 3.9 g of expected product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06794415B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-f9b2778d263b46429d3deb9aff87f0ff |
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| Source note | uspto-grants-2004_09 |
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