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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304354Generated: October 25, 2026

Hydrogen Peroxide → HCID 18435182, compound

https://huagongshe.com/reaction/2304354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantTrimethyl borateHCID 8470—
Reactant2,3-Difluoro-4'-octyloxybiphenylHCID 18435183—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18435182HCID 1843518269%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of n-butyllithium (1.60 ml, 10.0 M in hexanes, 0.016 mol) was added dropwise to a stirred, cooled (−78° C.) solution of 2,3-difluoro-4′-octyloxybiphenyl [see M. Hird and K. L. Toyne, J. Mater. Chem., 1995, 5, 2239] (4.70 g, 0.015 mol) in dry THF (250 ml) under dry nitrogen. The mixture was stirred at −78° C. for 2 hr and a solution of trimethyl borate (3.15 g, 0.030 mol) in dry THF (10 ml) was added. The mixture was allowed to warm to room temperature overnight and a solution of 30% hydrogen peroxide (50 ml) in acetic acid (500 ml) was added dropwise at room temperature. The mixture was extracted into ether (3 times) and the combined ethereal extracts were washed with water and dried over MgSO4. The solvent was removed in vacuo and the residue was recrystallised from ethanol to yield colourless crystals (3.45 g, 69%), mp 145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06436312B1
Source datasetuspto-grants-2002_08
ORD IDord-5b23c340e50e43f18ab0ae7845cc1022
Source noteuspto-grants-2002_08