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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674437Generated: October 30, 2026

Hydrogen Peroxide → HCID 178455779, compound

https://huagongshe.com/reaction/1674437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantTrimethyl borateHCID 8470—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178455776HCID 178455776—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178455779HCID 17845577950.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

37 g of 2,3-difluoro-1-(trans-4-ethylcyclohexyl)methoxybenzene was dissolved in 222 mL of THF, and 59.9 mL of butyllithium (2.67 M hexane solution) was added dropwise thereto at an internal temperature of −40° C. or lower. Then, further stirring was continued for 30 min. To this solution, 18.1 g of trimethyl borate was added dropwise at an internal temperature of −40° C. or lower, and then the temperature was increased to 0° C. Then, 24.7 mL of 30% hydrogen peroxide solution was added dropwise for 5 min, and the stirring was continued for 3 hours. Water and toluene were added thereto, and the organic layer was fractioned while the aqueous layer was extracted with toluene. The organic layers were combined and washed with water, and then the solvent was evaporated under reduced pressure. The obtained residue was purified by column chromatography, to thereby obtain 20 g of 2,3-difluoro-4-(trans-4-ethylcyclohexyl)methoxyphenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003006B2
Source datasetuspto-grants-2011_08
ORD IDord-8ff1c2e48b7e4e9b88097487ba678c1b
Source noteuspto-grants-2011_08