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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712203Generated: October 26, 2026

Triphenylphosphine → 5-Bromo-1,3-difluoro-2-[(octan-2-yl)oxy]benzene

https://huagongshe.com/reaction/1712203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant(+)-2-OctanolHCID 2723888—
Reactant4-Bromo-2,6-difluorophenolHCID 2736292—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-1,3-difluoro-2-[(octan-2-yl)oxy]benzeneHCID 68499982—

Reaction Steps

12.0 g of 4-bromo-2,6-difluorophenol, 10.0 ml of (S)-(+)-2-octanol and 16.5 g of triphenylphosphine were dissolved in 300 ml of tetrahydrofuran at about 20° C. with stirring under a nitrogen atmosphere. 12.5 ml of anhydrous (max. 0.0075% of H2O) diisopropyl azodicarboxylate were subsequently added dropwise. The reaction proceeds exothermically. The rate of addition was selected in such a way that the temperature of the mixture did not exceed 45° C. The reaction solution was subsequently stirred for 2 h, and the solvent was then removed in a rotary evaporator. The crude product was purified in a mixture of chlorobutane and heptane in the ratio 1:1 over 2 l of silica gel, giving 14.5 g of 3,5-difluoro-4-(1-methylheptyloxy)bromobenzene as a clear liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790929B2
Source datasetuspto-grants-2010_09
ORD IDord-9693b3f43740458d867d347e8f2aae7b
Source noteuspto-grants-2010_09