HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37618Generated: October 25, 2026
Water → 4-(Bromomethyl)phenylboronic acid
https://huagongshe.com/reaction/37618
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Tolylboronic acid | HCID 79799 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | 1,1,1-Trichloroethane | HCID 6278 | — |
| Product | 4-(Bromomethyl)phenylboronic acid | HCID 2735593 | 67.5% |
Reaction Steps
A mixture of 4-methylphenylboronic acid (27.2 g; 0.2 mole) in methyl chloroform (250 ml) was heated at reflux with azeotropic removal of water until approximately 2.5 ml of water was collected and a crystalline slurry was formed. A solution of azo(bisisobutyronitrile) (1.0 g) and bromine (32 g) in methyl chloroform (25 ml) was added to the refluxing slurry over 2-3 hours. The mixture was then refluxed until the bromine colour was discharged. The reaction mixture was allowed to cool and stirred at 10°-15° C. for 30 minutes. The suspended solid was collected by filtration, washed with methyl chloroform (2×50 ml) and dried at ambient temperature to give the anhydride of 4-bromomethylphenylboronic acid (29 g) (Compound F) as a white, crystalline solid, which was used without further purification or characterisation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05420292 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-8661317d4f8d49b68db114f65a279bdf |
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| Source note | uspto-grants-1995_05 |
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