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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566151Generated: October 29, 2026

Hydrochloric Acid → p-Octylphenylboric acid

https://huagongshe.com/reaction/566151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethyl borateHCID 8470—
Reactantp-BromophenyloctaneHCID 142854—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Productp-Octylphenylboric acidHCID 22728720—

Reaction Conditions

Temperature-78 °C

Reaction Steps

50 ml of THF (tetrahydrofuran) was added to 2.91 g (0.12 mol) of metallic magnesium, and the mixture was stirred. 100 ml of a solution of 26.89 g (0.1 mol) of p-octylbromobenzene in THF was added dropwise thereto, and the mixture was heated. After the initiation of the reaction was confirmed, the mixture was refluxed for one hr. The mixture was cooled to −78° C., 12.46 g (0.12 mol) of trimethylboric acid was added dropwise thereto, and the mixture was stirred for 30 min. The temperature was returned to room temperature, followed by stirring for additional one hr. Dilute hydrochloric acid was added thereto, and the mixture was stirred for one hr. The aqueous layer was extracted with ether, and the oil layer was washed with water and then with an aqueous sodium hydrogencarbonate. The oil layer was then dried over sodium sulfate, the solvent was removed by distillation, and the resultant crude product was purified by chromatography on silica gel to give p-octylphenylboric acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174455B1
Source datasetuspto-grants-2001_01
ORD IDord-dbec040289ef4a3ba7dcd60cd7963b48
Source noteuspto-grants-2001_01