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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864816Generated: October 25, 2026

Hydrogen Peroxide → Benzyl 5-hydroxy-2,2-dimethylpentanoate

https://huagongshe.com/reaction/1864816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
ReactantSodium AcetateHCID 517045—
ReactantBenzyl 2,2-dimethylpent-4-enoateHCID 66973286—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 5-hydroxy-2,2-dimethylpentanoateHCID 66972971—

Reaction Steps

To a solution of benzyl 2,2-dimethylpent-4-enoate (5.74 g, 26.3 mmol, prepared according to Step A) in THF (100 mL) was added a solution of 9-BBN (63.1 mL, 31.6 mmol, 0.5 M in THF) over 20 minutes, while under nitrogen. The reaction was allowed to stir at ambient temperature for 17 hours. An aqueous solution of sodium acetate (7.3 g, 89 mmol, in 18 mL of water) was then added, followed by the slow addition of aqueous hydrogen peroxide (18 mL, 30% by weight solution) with occasional chilling in a 0° C. bath. This mixture was allowed to stir at ambient temperature for 1.5 hours, before being extracted with ethyl acetate. The combined organics were washed with saturated brine. The organics were then dried over sodium sulfate, filtered, and concentrated in vacuo to give a residue that was purified by silica gel chromatography, eluting with a gradient of MeOH:DCM-1:99 to 10:90, to give the title compound. MS: m/z=237 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625901B2
Source datasetuspto-grants-2009_12
ORD IDord-0e41c0dd9e624322af6fc903a2f306a8
Source noteuspto-grants-2009_12