HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279586Generated: October 31, 2026
Sulfuric Acid → (4-Methoxyphenyl)boronic acid
https://huagongshe.com/reaction/1279586
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 ofanhydrous 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 containing 11 ml of sulphuric acid and 50 g of ice and water and agitation is carried out for 1 hour. The organic phase is extracted with 100 ml of a saturated aqueous solution of sodium bicarbonate, the aqueous phases are combined, 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 | US06448294B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-ee951f7b321e4aefa509bb41e82411e0 |
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| Source note | uspto-grants-2002_09 |
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