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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827294Generated: October 30, 2026

Hydrogen Peroxide → HCID 22136233, compound

https://huagongshe.com/reaction/1827294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantHexaneHCID 8058—
ReactantSodium HydroxideHCID 14798—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
ReactantHCID 54572837HCID 54572837—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22136233HCID 22136233—

Reaction Steps

To a solution of 0.4 M 9-BBN in hexane (72 mL, 28.8 mmol) was added 4-bromophenyl-1-butene (3.99 g, 18.9 mmol) at room temperature. The resulting mixture was stirred at room temperature for 20 h. The mixture was treated sequentially with 3.3 mL of 6N aqueous NaOH (19.8 mmol), THF (7 mL), and 30% H2O2 in H2O (7 mL), then refluxed for 2 h. The reaction mixture was then cooled to room temperature. The organic layer was washed with aqueous sodium sulfite (40 mL), H2O (20 mL), and brine (20 mL). The aqueous extracts were combined, saturated with solid K2CO3 and extracted with Et2O (3×50 mL). The combined organic extracts were dried over Na2 SO4, filtered and concentrated. The resulting crude product was purified by flash chromatography twice (33% EtOAc in hexane and 20% EtOAc in hexane) to yield 4-(o-bromophenyl)butanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053101B2
Source datasetuspto-grants-2006_05
ORD IDord-72f692e7e04f48b39f9995aa09c4becd
Source noteuspto-grants-2006_05